Canonical Allele Identifier: CA367396786

Gene: GCK

Linked Data

• gnomAD v4: 7-44145155-G-T
• MyVariant Identifiers: chr7:g.44184754G>T (hg19) ; chr7:g.44145155G>T (hg38)

Genomic Alleles

HGVS	Genome Assembly
NC_000007.14:g.44145155G>T , CM000669.2:g.44145155G>T	GRCh38
NC_000007.13:g.44184754G>T , CM000669.1:g.44184754G>T	GRCh37
NC_000007.12:g.44151279G>T	NCBI36
NG_008847.1:g.49269C>A
NG_008847.2:g.58016C>A

Transcript Alleles

HGVS	Amino-acid Change
ENST00000395796.8:c.*1377C>A	ENSP00000379142.4:n.*1377C>A
ENST00000616242.5:c.*499C>A	ENSP00000482149.2:n.*499C>A
ENST00000683378.1:n.605C>A
ENST00000336642.9:c.413C>A	ENSP00000338009.5:p.Ala138Asp
ENST00000345378.7:c.1382C>A	ENSP00000223366.2:p.Ala461Asp
ENST00000403799.8:c.1379C>A MANE Select	ENSP00000384247.3:p.Ala460Asp
ENST00000671824.1:c.1442C>A	ENSP00000500264.1:p.Ala481Asp
ENST00000672743.1:n.381+10C>A
ENST00000673284.1:c.1369+10C>A	ENSP00000499852.1:n.1369+10C>A
ENST00000336642.8:c.431C>A	ENSP00000338009.4:p.Ala144Asp
ENST00000345378.6:c.1382C>A	ENSP00000223366.2:p.Ala461Asp
ENST00000395796.7:c.1376C>A	ENSP00000379142.3:p.Ala459Asp
ENST00000403799.7:c.1379C>A	ENSP00000384247.3:p.Ala460Asp
ENST00000437084.1:c.1328C>A	ENSP00000402840.1:p.Ala443Asp
ENST00000459642.1:n.759C>A
ENST00000616242.4:c.1376C>A	ENSP00000482149.1:p.Ala459Asp
NM_000162.3:c.1379C>A	NP_000153.1:p.Ala460Asp
NM_033507.1:c.1382C>A	NP_277042.1:p.Ala461Asp
NM_033508.1:c.1376C>A	NP_277043.1:p.Ala459Asp
NM_000162.4:c.1379C>A	NP_000153.1:p.Ala460Asp
NM_001354800.1:c.1369+10C>A	NP_001341729.1:n.1369+10C>A
NM_001354801.1:c.368C>A	NP_001341730.1:p.Ala123Asp
NM_001354802.1:c.229+10C>A	NP_001341731.1:n.229+10C>A
NM_001354803.1:c.413C>A	NP_001341732.1:p.Ala138Asp
NM_033507.2:c.1382C>A	NP_277042.1:p.Ala461Asp
NM_033508.2:c.1376C>A	NP_277043.1:p.Ala459Asp
XM_024446707.1:c.239C>A	XP_024302475.1:p.Ala80Asp
NM_000162.5:c.1379C>A MANE Select	NP_000153.1:p.Ala460Asp
NM_033507.3:c.1382C>A	NP_277042.1:p.Ala461Asp
NM_033508.3:c.1376C>A	NP_277043.1:p.Ala459Asp
NM_001354803.2:c.413C>A	NP_001341732.1:p.Ala138Asp