Canonical Allele Identifier: CA367400555
Gene: GCK HGNC NCBI

Linked Data

COSMIC: COSM746812 COSM746813 COSM4861275
MyVariant Identifiers: chr7:g.44187324G>A (hg19) chr7:g.44147725G>A (hg38)
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Genomic Alleles

HGVS Genome Assembly
NC_000007.14:g.44147725G>A , CM000669.2:g.44147725G>A GRCh38
NC_000007.13:g.44187324G>A , CM000669.1:g.44187324G>A GRCh37
NC_000007.12:g.44153849G>A NCBI36
NG_008847.1:g.46699C>T
NG_008847.2:g.55446C>T

Transcript Alleles

HGVS Amino-acid Change
ENST00000395796.8:c.*786C>T ENSP00000379142.4:n.*786C>T
ENST00000616242.5:c.788C>T ENSP00000482149.2:p.Ser263Phe
ENST00000345378.7:c.791C>T ENSP00000223366.2:p.Ser264Phe
ENST00000403799.8:c.788C>T MANE Select ENSP00000384247.3:p.Ser263Phe
ENST00000671824.1:c.788C>T ENSP00000500264.1:p.Ser263Phe
ENST00000673284.1:c.788C>T ENSP00000499852.1:p.Ser263Phe
ENST00000345378.6:c.791C>T ENSP00000223366.2:p.Ser264Phe
ENST00000395796.7:c.785C>T ENSP00000379142.3:p.Ser262Phe
ENST00000403799.7:c.788C>T ENSP00000384247.3:p.Ser263Phe
ENST00000437084.1:c.737C>T ENSP00000402840.1:p.Ser246Phe
ENST00000616242.4:c.785C>T ENSP00000482149.1:p.Ser262Phe
NM_000162.3:c.788C>T NP_000153.1:p.Ser263Phe
NM_033507.1:c.791C>T NP_277042.1:p.Ser264Phe
NM_033508.1:c.785C>T NP_277043.1:p.Ser262Phe
XR_927223.1:n.59G>A
NM_000162.4:c.788C>T NP_000153.1:p.Ser263Phe
NM_001354800.1:c.788C>T NP_001341729.1:p.Ser263Phe
NM_033507.2:c.791C>T NP_277042.1:p.Ser264Phe
NM_033508.2:c.785C>T NP_277043.1:p.Ser262Phe
XR_927223.2:n.59G>A
NM_000162.5:c.788C>T MANE Select NP_000153.1:p.Ser263Phe
NM_033507.3:c.791C>T NP_277042.1:p.Ser264Phe
NM_033508.3:c.785C>T NP_277043.1:p.Ser262Phe
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