Canonical Allele Identifier: CA2714140971

Gene: GCK

Linked Data

• dbSNP Id: rs748161171

Genomic Alleles

HGVS	Genome Assembly
NC_000007.14:g.44149946G>T , CM000669.2:g.44149946G>T	GRCh38
NC_000007.13:g.44189545G>T , CM000669.1:g.44189545G>T	GRCh37
NC_000007.12:g.44156070G>T	NCBI36
NG_008847.1:g.44478C>A
NG_008847.2:g.53225C>A

Transcript Alleles

HGVS	Amino-acid Change
ENST00000395796.8:c.*577+23C>A	ENSP00000379142.4:n.*577+23C>A
ENST00000616242.5:c.579+23C>A	ENSP00000482149.2:n.579+23C>A
ENST00000682635.1:n.1065+23C>A
ENST00000345378.7:c.582+23C>A	ENSP00000223366.2:n.582+23C>A
ENST00000403799.8:c.579+23C>A MANE Select	ENSP00000384247.3:n.579+23C>A
ENST00000671824.1:c.579+23C>A	ENSP00000500264.1:n.579+23C>A
ENST00000673284.1:c.579+23C>A	ENSP00000499852.1:n.579+23C>A
ENST00000345378.6:c.582+23C>A	ENSP00000223366.2:n.582+23C>A
ENST00000395796.7:c.576+23C>A	ENSP00000379142.3:n.576+23C>A
ENST00000403799.7:c.579+23C>A	ENSP00000384247.3:n.579+23C>A
ENST00000437084.1:c.528+23C>A	ENSP00000402840.1:n.528+23C>A
ENST00000616242.4:c.576+23C>A	ENSP00000482149.1:n.576+23C>A
NM_000162.3:c.579+23C>A	NP_000153.1:n.579+23C>A
NM_033507.1:c.582+23C>A	NP_277042.1:n.582+23C>A
NM_033508.1:c.576+23C>A	NP_277043.1:n.576+23C>A
NM_000162.4:c.579+23C>A	NP_000153.1:n.579+23C>A
NM_001354800.1:c.579+23C>A	NP_001341729.1:n.579+23C>A
NM_033507.2:c.582+23C>A	NP_277042.1:n.582+23C>A
NM_033508.2:c.576+23C>A	NP_277043.1:n.576+23C>A
NM_000162.5:c.579+23C>A MANE Select	NP_000153.1:n.579+23C>A
NM_033507.3:c.582+23C>A	NP_277042.1:n.582+23C>A
NM_033508.3:c.576+23C>A	NP_277043.1:n.576+23C>A