Canonical Allele Identifier: CA1703612826

Gene: GCK

Genomic Alleles

HGVS	Genome Assembly
NC_000007.14:g.44145476G= , CM000669.2:g.44145476G=	GRCh38
NC_000007.13:g.44185075G= , CM000669.1:g.44185075G=	GRCh37
NC_000007.12:g.44151600G=	NCBI36
NG_008847.1:g.48948C=
NG_008847.2:g.57695C=

Transcript Alleles

HGVS	Amino-acid Change
ENST00000395796.8:c.*1251+21C=	ENSP00000379142.4:n.*1251+21C=
ENST00000616242.5:c.*373+21C=	ENSP00000482149.2:n.*373+21C=
ENST00000683378.1:n.479+21C=
ENST00000336642.9:c.287+21C=	ENSP00000338009.5:n.287+21C=
ENST00000345378.7:c.1256+21C=	ENSP00000223366.2:n.1256+21C=
ENST00000403799.8:c.1253+21C= MANE Select	ENSP00000384247.3:n.1253+21C=
ENST00000671824.1:c.1316+21C=	ENSP00000500264.1:n.1316+21C=
ENST00000672743.1:n.265+21C=
ENST00000673284.1:c.1253+21C=	ENSP00000499852.1:n.1253+21C=
ENST00000336642.8:c.305+21C=	ENSP00000338009.4:n.305+21C=
ENST00000345378.6:c.1256+21C=	ENSP00000223366.2:n.1256+21C=
ENST00000395796.7:c.1250+21C=	ENSP00000379142.3:n.1250+21C=
ENST00000403799.7:c.1253+21C=	ENSP00000384247.3:n.1253+21C=
ENST00000437084.1:c.1202+21C=	ENSP00000402840.1:n.1202+21C=
ENST00000459642.1:n.633+21C=
ENST00000616242.4:c.1250+21C=	ENSP00000482149.1:n.1250+21C=
NM_000162.3:c.1253+21C=	NP_000153.1:n.1253+21C=
NM_033507.1:c.1256+21C=	NP_277042.1:n.1256+21C=
NM_033508.1:c.1250+21C=	NP_277043.1:n.1250+21C=
NM_000162.4:c.1253+21C=	NP_000153.1:n.1253+21C=
NM_001354800.1:c.1253+21C=	NP_001341729.1:n.1253+21C=
NM_001354801.1:c.242+21C=	NP_001341730.1:n.242+21C=
NM_001354802.1:c.113+21C=	NP_001341731.1:n.113+21C=
NM_001354803.1:c.287+21C=	NP_001341732.1:n.287+21C=
NM_033507.2:c.1256+21C=	NP_277042.1:n.1256+21C=
NM_033508.2:c.1250+21C=	NP_277043.1:n.1250+21C=
XM_024446707.1:c.113+21C=	XP_024302475.1:n.113+21C=
NM_000162.5:c.1253+21C= MANE Select	NP_000153.1:n.1253+21C=
NM_033507.3:c.1256+21C=	NP_277042.1:n.1256+21C=
NM_033508.3:c.1250+21C=	NP_277043.1:n.1250+21C=
NM_001354803.2:c.287+21C=	NP_001341732.1:n.287+21C=