Canonical Allele Identifier: CA1703612690

Gene: GCK

Genomic Alleles

HGVS	Genome Assembly
NC_000007.14:g.44145240G= , CM000669.2:g.44145240G=	GRCh38
NC_000007.13:g.44184839G= , CM000669.1:g.44184839G=	GRCh37
NC_000007.12:g.44151364G=	NCBI36
NG_008847.1:g.49184C=
NG_008847.2:g.57931C=

Transcript Alleles

HGVS	Amino-acid Change
ENST00000395796.8:c.*1292C=	ENSP00000379142.4:n.*1292C=
ENST00000616242.5:c.*414C=	ENSP00000482149.2:n.*414C=
ENST00000683378.1:n.520C=
ENST00000336642.9:c.328C=	ENSP00000338009.5:p.Pro110=
ENST00000345378.7:c.1297C=	ENSP00000223366.2:p.Pro433=
ENST00000403799.8:c.1294C= MANE Select	ENSP00000384247.3:p.Pro432=
ENST00000671824.1:c.1357C=	ENSP00000500264.1:p.Pro453=
ENST00000672743.1:n.306C=
ENST00000673284.1:c.1294C=	ENSP00000499852.1:p.Pro432=
ENST00000336642.8:c.346C=	ENSP00000338009.4:p.Pro116=
ENST00000345378.6:c.1297C=	ENSP00000223366.2:p.Pro433=
ENST00000395796.7:c.1291C=	ENSP00000379142.3:p.Pro431=
ENST00000403799.7:c.1294C=	ENSP00000384247.3:p.Pro432=
ENST00000437084.1:c.1243C=	ENSP00000402840.1:p.Pro415=
ENST00000459642.1:n.674C=
ENST00000616242.4:c.1291C=	ENSP00000482149.1:p.Pro431=
NM_000162.3:c.1294C=	NP_000153.1:p.Pro432=
NM_033507.1:c.1297C=	NP_277042.1:p.Pro433=
NM_033508.1:c.1291C=	NP_277043.1:p.Pro431=
NM_000162.4:c.1294C=	NP_000153.1:p.Pro432=
NM_001354800.1:c.1294C=	NP_001341729.1:p.Pro432=
NM_001354801.1:c.283C=	NP_001341730.1:p.Pro95=
NM_001354802.1:c.154C=	NP_001341731.1:p.Pro52=
NM_001354803.1:c.328C=	NP_001341732.1:p.Pro110=
NM_033507.2:c.1297C=	NP_277042.1:p.Pro433=
NM_033508.2:c.1291C=	NP_277043.1:p.Pro431=
XM_024446707.1:c.154C=	XP_024302475.1:p.Pro52=
NM_000162.5:c.1294C= MANE Select	NP_000153.1:p.Pro432=
NM_033507.3:c.1297C=	NP_277042.1:p.Pro433=
NM_033508.3:c.1291C=	NP_277043.1:p.Pro431=
NM_001354803.2:c.328C=	NP_001341732.1:p.Pro110=