Canonical Allele Identifier: CA367401247
Gene: GCK HGNC NCBI

Linked Data

MyVariant Identifiers: chr7:g.44189394T>C (hg19) chr7:g.44149795T>C (hg38)
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Genomic Alleles

HGVS Genome Assembly
NC_000007.14:g.44149795T>C , CM000669.2:g.44149795T>C GRCh38
NC_000007.13:g.44189394T>C , CM000669.1:g.44189394T>C GRCh37
NC_000007.12:g.44155919T>C NCBI36
NG_008847.1:g.44629A>G
NG_008847.2:g.53376A>G

Transcript Alleles

HGVS Amino-acid Change
ENST00000395796.8:c.*642A>G ENSP00000379142.4:n.*642A>G
ENST00000616242.5:c.644A>G ENSP00000482149.2:p.Tyr215Cys
ENST00000682635.1:n.1130A>G
ENST00000345378.7:c.647A>G ENSP00000223366.2:p.Tyr216Cys
ENST00000403799.8:c.644A>G MANE Select ENSP00000384247.3:p.Tyr215Cys
ENST00000671824.1:c.644A>G ENSP00000500264.1:p.Tyr215Cys
ENST00000673284.1:c.644A>G ENSP00000499852.1:p.Tyr215Cys
ENST00000345378.6:c.647A>G ENSP00000223366.2:p.Tyr216Cys
ENST00000395796.7:c.641A>G ENSP00000379142.3:p.Tyr214Cys
ENST00000403799.7:c.644A>G ENSP00000384247.3:p.Tyr215Cys
ENST00000437084.1:c.593A>G ENSP00000402840.1:p.Tyr198Cys
ENST00000616242.4:c.641A>G ENSP00000482149.1:p.Tyr214Cys
NM_000162.3:c.644A>G NP_000153.1:p.Tyr215Cys
NM_033507.1:c.647A>G NP_277042.1:p.Tyr216Cys
NM_033508.1:c.641A>G NP_277043.1:p.Tyr214Cys
NM_000162.4:c.644A>G NP_000153.1:p.Tyr215Cys
NM_001354800.1:c.644A>G NP_001341729.1:p.Tyr215Cys
NM_033507.2:c.647A>G NP_277042.1:p.Tyr216Cys
NM_033508.2:c.641A>G NP_277043.1:p.Tyr214Cys
NM_000162.5:c.644A>G MANE Select NP_000153.1:p.Tyr215Cys
NM_033507.3:c.647A>G NP_277042.1:p.Tyr216Cys
NM_033508.3:c.641A>G NP_277043.1:p.Tyr214Cys
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