Canonical Allele Identifier: CA1703635920

Gene: GCK

Linked Data

• dbSNP Id: rs948353492

Genomic Alleles

HGVS	Genome Assembly
NC_000007.14:g.44149922T>G , CM000669.2:g.44149922T>G	GRCh38
NC_000007.13:g.44189521T>G , CM000669.1:g.44189521T>G	GRCh37
NC_000007.12:g.44156046T>G	NCBI36
NG_008847.1:g.44502A>C
NG_008847.2:g.53249A>C

Transcript Alleles

HGVS	Amino-acid change
ENST00000395796.8:c.*577+47A>C	ENSP00000379142.4:n.*577+47A>C
ENST00000616242.5:c.579+47A>C	ENSP00000482149.2:n.579+47A>C
ENST00000682635.1:n.1065+47A>C
ENST00000345378.7:c.582+47A>C	ENSP00000223366.2:n.582+47A>C
ENST00000403799.8:c.579+47A>C MANE Select	ENSP00000384247.3:n.579+47A>C
ENST00000671824.1:c.579+47A>C	ENSP00000500264.1:n.579+47A>C
ENST00000673284.1:c.579+47A>C	ENSP00000499852.1:n.579+47A>C
ENST00000345378.6:c.582+47A>C	ENSP00000223366.2:n.582+47A>C
ENST00000395796.7:c.576+47A>C	ENSP00000379142.3:n.576+47A>C
ENST00000403799.7:c.579+47A>C	ENSP00000384247.3:n.579+47A>C
ENST00000437084.1:c.528+47A>C	ENSP00000402840.1:n.528+47A>C
ENST00000616242.4:c.576+47A>C	ENSP00000482149.1:n.576+47A>C
NM_000162.3:c.579+47A>C	NP_000153.1:n.579+47A>C
NM_033507.1:c.582+47A>C	NP_277042.1:n.582+47A>C
NM_033508.1:c.576+47A>C	NP_277043.1:n.576+47A>C
NM_000162.4:c.579+47A>C	NP_000153.1:n.579+47A>C
NM_001354800.1:c.579+47A>C	NP_001341729.1:n.579+47A>C
NM_033507.2:c.582+47A>C	NP_277042.1:n.582+47A>C
NM_033508.2:c.576+47A>C	NP_277043.1:n.576+47A>C
NM_000162.5:c.579+47A>C MANE Select	NP_000153.1:n.579+47A>C
NM_033507.3:c.582+47A>C	NP_277042.1:n.582+47A>C
NM_033508.3:c.576+47A>C	NP_277043.1:n.576+47A>C