Canonical Allele Identifier: CA367400286
Gene: GCK HGNC NCBI

Linked Data

MyVariant Identifiers: chr7:g.44186219T>G (hg19) chr7:g.44146620T>G (hg38)
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Genomic Alleles

HGVS Genome Assembly
NC_000007.14:g.44146620T>G , CM000669.2:g.44146620T>G GRCh38
NC_000007.13:g.44186219T>G , CM000669.1:g.44186219T>G GRCh37
NC_000007.12:g.44152744T>G NCBI36
NG_008847.1:g.47804A>C
NG_008847.2:g.56551A>C

Transcript Alleles

HGVS Amino-acid Change
ENST00000395796.8:c.*862-2A>C ENSP00000379142.4:n.*862-2A>C
ENST00000616242.5:c.854-2A>C ENSP00000482149.2:n.854-2A>C
ENST00000683378.1:n.88A>C
ENST00000345378.7:c.867-2A>C ENSP00000223366.2:n.867-2A>C
ENST00000403799.8:c.864-2A>C MANE Select ENSP00000384247.3:n.864-2A>C
ENST00000671824.1:c.927-2A>C ENSP00000500264.1:n.927-2A>C
ENST00000673284.1:c.864-2A>C ENSP00000499852.1:n.864-2A>C
ENST00000345378.6:c.867-2A>C ENSP00000223366.2:n.867-2A>C
ENST00000395796.7:c.861-2A>C ENSP00000379142.3:n.861-2A>C
ENST00000403799.7:c.864-2A>C ENSP00000384247.3:n.864-2A>C
ENST00000437084.1:c.813-2A>C ENSP00000402840.1:n.813-2A>C
ENST00000473353.1:n.162-2A>C
ENST00000616242.4:c.861-2A>C ENSP00000482149.1:n.861-2A>C
NM_000162.3:c.864-2A>C NP_000153.1:n.864-2A>C
NM_033507.1:c.867-2A>C NP_277042.1:n.867-2A>C
NM_033508.1:c.861-2A>C NP_277043.1:n.861-2A>C
NM_000162.4:c.864-2A>C NP_000153.1:n.864-2A>C
NM_001354800.1:c.864-2A>C NP_001341729.1:n.864-2A>C
NM_001354801.1:c.7A>C NP_001341730.1:p.Ser3Arg
NM_033507.2:c.867-2A>C NP_277042.1:n.867-2A>C
NM_033508.2:c.861-2A>C NP_277043.1:n.861-2A>C
NM_000162.5:c.864-2A>C MANE Select NP_000153.1:n.864-2A>C
NM_033507.3:c.867-2A>C NP_277042.1:n.867-2A>C
NM_033508.3:c.861-2A>C NP_277043.1:n.861-2A>C
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