Canonical Allele Identifier: CA367396836

Gene: GCK

Linked Data

• gnomAD v4: 7-44145164-C-T
• MyVariant Identifiers: chr7:g.44184763C>T (hg19) ; chr7:g.44145164C>T (hg38)

Genomic Alleles

HGVS	Genome Assembly
NC_000007.14:g.44145164C>T , CM000669.2:g.44145164C>T	GRCh38
NC_000007.13:g.44184763C>T , CM000669.1:g.44184763C>T	GRCh37
NC_000007.12:g.44151288C>T	NCBI36
NG_008847.1:g.49260G>A
NG_008847.2:g.58007G>A

Transcript Alleles

HGVS	Amino-acid change
ENST00000395796.8:c.*1368G>A	ENSP00000379142.4:n.*1368G>A
ENST00000616242.5:c.*490G>A	ENSP00000482149.2:n.*490G>A
ENST00000683378.1:n.596G>A
ENST00000336642.9:c.404G>A	ENSP00000338009.5:p.Cys135Tyr
ENST00000345378.7:c.1373G>A	ENSP00000223366.2:p.Cys458Tyr
ENST00000403799.8:c.1370G>A MANE Select	ENSP00000384247.3:p.Cys457Tyr
ENST00000671824.1:c.1433G>A	ENSP00000500264.1:p.Cys478Tyr
ENST00000672743.1:n.381+1G>A
ENST00000673284.1:c.1369+1G>A	ENSP00000499852.1:n.1369+1G>A
ENST00000336642.8:c.422G>A	ENSP00000338009.4:p.Cys141Tyr
ENST00000345378.6:c.1373G>A	ENSP00000223366.2:p.Cys458Tyr
ENST00000395796.7:c.1367G>A	ENSP00000379142.3:p.Cys456Tyr
ENST00000403799.7:c.1370G>A	ENSP00000384247.3:p.Cys457Tyr
ENST00000437084.1:c.1319G>A	ENSP00000402840.1:p.Cys440Tyr
ENST00000459642.1:n.750G>A
ENST00000616242.4:c.1367G>A	ENSP00000482149.1:p.Cys456Tyr
NM_000162.3:c.1370G>A	NP_000153.1:p.Cys457Tyr
NM_033507.1:c.1373G>A	NP_277042.1:p.Cys458Tyr
NM_033508.1:c.1367G>A	NP_277043.1:p.Cys456Tyr
NM_000162.4:c.1370G>A	NP_000153.1:p.Cys457Tyr
NM_001354800.1:c.1369+1G>A	NP_001341729.1:n.1369+1G>A
NM_001354801.1:c.359G>A	NP_001341730.1:p.Cys120Tyr
NM_001354802.1:c.229+1G>A	NP_001341731.1:n.229+1G>A
NM_001354803.1:c.404G>A	NP_001341732.1:p.Cys135Tyr
NM_033507.2:c.1373G>A	NP_277042.1:p.Cys458Tyr
NM_033508.2:c.1367G>A	NP_277043.1:p.Cys456Tyr
XM_024446707.1:c.230G>A	XP_024302475.1:p.Cys77Tyr
NM_000162.5:c.1370G>A MANE Select	NP_000153.1:p.Cys457Tyr
NM_033507.3:c.1373G>A	NP_277042.1:p.Cys458Tyr
NM_033508.3:c.1367G>A	NP_277043.1:p.Cys456Tyr
NM_001354803.2:c.404G>A	NP_001341732.1:p.Cys135Tyr