Canonical Allele Identifier: CA1703612629

Gene: GCK

Genomic Alleles

HGVS	Genome Assembly
NC_000007.14:g.44145121T= , CM000669.2:g.44145121T=	GRCh38
NC_000007.13:g.44184720T= , CM000669.1:g.44184720T=	GRCh37
NC_000007.12:g.44151245T=	NCBI36
NG_008847.1:g.49303A=
NG_008847.2:g.58050A=

Transcript Alleles

HGVS	Amino-acid Change
ENST00000395796.8:c.*1411A=	ENSP00000379142.4:n.*1411A=
ENST00000616242.5:c.*533A=	ENSP00000482149.2:n.*533A=
ENST00000683378.1:n.639A=
ENST00000336642.9:c.*15A=	ENSP00000338009.5:n.*15A=
ENST00000345378.7:c.*15A=	ENSP00000223366.2:n.*15A=
ENST00000403799.8:c.*15A= MANE Select	ENSP00000384247.3:n.*15A=
ENST00000671824.1:c.*15A=	ENSP00000500264.1:n.*15A=
ENST00000672743.1:n.381+44A=
ENST00000673284.1:c.1369+44A=	ENSP00000499852.1:n.1369+44A=
ENST00000336642.8:c.465A=	ENSP00000338009.4:n.465A=
ENST00000345378.6:c.*15A=	ENSP00000223366.2:n.*15A=
ENST00000395796.7:c.*15A=	ENSP00000379142.3:n.*15A=
ENST00000403799.7:c.*15A=	ENSP00000384247.3:n.*15A=
ENST00000459642.1:n.793A=
ENST00000616242.4:c.1410A=	ENSP00000482149.1:n.1410A=
NM_000162.3:c.*15A=	NP_000153.1:n.*15A=
NM_033507.1:c.*15A=	NP_277042.1:n.*15A=
NM_033508.1:c.*15A=	NP_277043.1:n.*15A=
NM_000162.4:c.*15A=	NP_000153.1:n.*15A=
NM_001354800.1:c.1369+44A=	NP_001341729.1:n.1369+44A=
NM_001354801.1:c.*15A=	NP_001341730.1:n.*15A=
NM_001354802.1:c.229+44A=	NP_001341731.1:n.229+44A=
NM_001354803.1:c.*15A=	NP_001341732.1:n.*15A=
NM_033507.2:c.*15A=	NP_277042.1:n.*15A=
NM_033508.2:c.*15A=	NP_277043.1:n.*15A=
XM_024446707.1:c.*15A=	XP_024302475.1:n.*15A=
NM_000162.5:c.*15A= MANE Select	NP_000153.1:n.*15A=
NM_033507.3:c.*15A=	NP_277042.1:n.*15A=
NM_033508.3:c.*15A=	NP_277043.1:n.*15A=
NM_001354803.2:c.*15A=	NP_001341732.1:n.*15A=