Canonical Allele Identifier: CA4239730
Gene: GCK HGNC NCBI

Linked Data

dbSNP Id: rs773409497
ExAC: 7:44193098 G / GTCCCCACACCATCCCACTGCCTTGATTCACACCCAGCCCACA
MyVariant Identifiers: chr7:g.44193098_44193099insTCCCCACACCATCCCACTGCCTTGATTCACACCCAGCCCACA (hg19) chr7:g.44153499_44153500insTCCCCACACCATCCCACTGCCTTGATTCACACCCAGCCCACA (hg38)
JSON-LD

Genomic Alleles

HGVS Genome Assembly
NC_000007.14:g.44153499_44153500insTCCCCACACCATCCCACTGCCTTGATTCACACCCAGCCCACA , CM000669.2:g.44153499_44153500insTCCCCACACCATCCCACTGCCTTGATTCACACCCAGCCCACA GRCh38
NC_000007.13:g.44193098_44193099insTCCCCACACCATCCCACTGCCTTGATTCACACCCAGCCCACA , CM000669.1:g.44193098_44193099insTCCCCACACCATCCCACTGCCTTGATTCACACCCAGCCCACA GRCh37
NC_000007.12:g.44159623_44159624insTCCCCACACCATCCCACTGCCTTGATTCACACCCAGCCCACA NCBI36
NG_008847.1:g.40924_40925insTGTGGGCTGGGTGTGAATCAAGGCAGTGGGATGGTGTGGGGA
NG_008847.2:g.49671_49672insTGTGGGCTGGGTGTGAATCAAGGCAGTGGGATGGTGTGGGGA

Transcript Alleles

HGVS Amino-acid Change
ENST00000395796.8:c.*44-37_*44-36insTGTGGGCTGGGTGTGAATCAAGGCAGTGGGATGGTGTGGGGA ENSP00000379142.4:n.*44-37_*44-36insTGTGGGCTGGGTGTGAATCAAGGCA...
ENST00000616242.5:c.46-37_46-36insTGTGGGCTGGGTGTGAATCAAGGCAGTGGGATGGTGTGGGGA ENSP00000482149.2:n.46-37_46-36insTGTGGGCTGGGTGTGAATCAAGGCAGT...
ENST00000682635.1:n.532-37_532-36insTGTGGGCTGGGTGTGAATCAAGGCAGTGGGATGGTGTGGGGA
ENST00000345378.7:c.49-37_49-36insTGTGGGCTGGGTGTGAATCAAGGCAGTGGGATGGTGTGGGGA ENSP00000223366.2:n.49-37_49-36insTGTGGGCTGGGTGTGAATCAAGGCAGT...
ENST00000403799.8:c.46-37_46-36insTGTGGGCTGGGTGTGAATCAAGGCAGTGGGATGGTGTGGGGA MANE Select ENSP00000384247.3:n.46-37_46-36insTGTGGGCTGGGTGTGAATCAAGGCAGT...
ENST00000671824.1:c.46-37_46-36insTGTGGGCTGGGTGTGAATCAAGGCAGTGGGATGGTGTGGGGA ENSP00000500264.1:n.46-37_46-36insTGTGGGCTGGGTGTGAATCAAGGCAGT...
ENST00000673284.1:c.46-37_46-36insTGTGGGCTGGGTGTGAATCAAGGCAGTGGGATGGTGTGGGGA ENSP00000499852.1:n.46-37_46-36insTGTGGGCTGGGTGTGAATCAAGGCAGT...
ENST00000345378.6:c.49-37_49-36insTGTGGGCTGGGTGTGAATCAAGGCAGTGGGATGGTGTGGGGA ENSP00000223366.2:n.49-37_49-36insTGTGGGCTGGGTGTGAATCAAGGCAGT...
ENST00000395796.7:c.43-37_43-36insTGTGGGCTGGGTGTGAATCAAGGCAGTGGGATGGTGTGGGGA ENSP00000379142.3:n.43-37_43-36insTGTGGGCTGGGTGTGAATCAAGGCAGT...
ENST00000403799.7:c.46-37_46-36insTGTGGGCTGGGTGTGAATCAAGGCAGTGGGATGGTGTGGGGA ENSP00000384247.3:n.46-37_46-36insTGTGGGCTGGGTGTGAATCAAGGCAGT...
ENST00000437084.1:c.46-37_46-36insTGTGGGCTGGGTGTGAATCAAGGCAGTGGGATGGTGTGGGGA ENSP00000402840.1:n.46-37_46-36insTGTGGGCTGGGTGTGAATCAAGGCAGT...
ENST00000476008.1:n.481-37_481-36insTGTGGGCTGGGTGTGAATCAAGGCAGTGGGATGGTGTGGGGA
ENST00000616242.4:c.43-37_43-36insTGTGGGCTGGGTGTGAATCAAGGCAGTGGGATGGTGTGGGGA ENSP00000482149.1:n.43-37_43-36insTGTGGGCTGGGTGTGAATCAAGGCAGT...
NM_000162.3:c.46-37_46-36insTGTGGGCTGGGTGTGAATCAAGGCAGTGGGATGGTGTGGGGA NP_000153.1:n.46-37_46-36insTGTGGGCTGGGTGTGAATCAAGGCAGTGGGATG...
NM_033507.1:c.49-37_49-36insTGTGGGCTGGGTGTGAATCAAGGCAGTGGGATGGTGTGGGGA NP_277042.1:n.49-37_49-36insTGTGGGCTGGGTGTGAATCAAGGCAGTGGGATG...
NM_033508.1:c.43-37_43-36insTGTGGGCTGGGTGTGAATCAAGGCAGTGGGATGGTGTGGGGA NP_277043.1:n.43-37_43-36insTGTGGGCTGGGTGTGAATCAAGGCAGTGGGATG...
NM_000162.4:c.46-37_46-36insTGTGGGCTGGGTGTGAATCAAGGCAGTGGGATGGTGTGGGGA NP_000153.1:n.46-37_46-36insTGTGGGCTGGGTGTGAATCAAGGCAGTGGGATG...
NM_001354800.1:c.46-37_46-36insTGTGGGCTGGGTGTGAATCAAGGCAGTGGGATGGTGTGGGGA NP_001341729.1:n.46-37_46-36insTGTGGGCTGGGTGTGAATCAAGGCAGTGGG...
NM_033507.2:c.49-37_49-36insTGTGGGCTGGGTGTGAATCAAGGCAGTGGGATGGTGTGGGGA NP_277042.1:n.49-37_49-36insTGTGGGCTGGGTGTGAATCAAGGCAGTGGGATG...
NM_033508.2:c.43-37_43-36insTGTGGGCTGGGTGTGAATCAAGGCAGTGGGATGGTGTGGGGA NP_277043.1:n.43-37_43-36insTGTGGGCTGGGTGTGAATCAAGGCAGTGGGATG...
NM_000162.5:c.46-37_46-36insTGTGGGCTGGGTGTGAATCAAGGCAGTGGGATGGTGTGGGGA MANE Select NP_000153.1:n.46-37_46-36insTGTGGGCTGGGTGTGAATCAAGGCAGTGGGATG...
NM_033507.3:c.49-37_49-36insTGTGGGCTGGGTGTGAATCAAGGCAGTGGGATGGTGTGGGGA NP_277042.1:n.49-37_49-36insTGTGGGCTGGGTGTGAATCAAGGCAGTGGGATG...
NM_033508.3:c.43-37_43-36insTGTGGGCTGGGTGTGAATCAAGGCAGTGGGATGGTGTGGGGA NP_277043.1:n.43-37_43-36insTGTGGGCTGGGTGTGAATCAAGGCAGTGGGATG...
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