Canonical Allele Identifier: CA1703612604

Gene: GCK

Genomic Alleles

HGVS	Genome Assembly
NC_000007.14:g.44145065G= , CM000669.2:g.44145065G=	GRCh38
NC_000007.13:g.44184664G= , CM000669.1:g.44184664G=	GRCh37
NC_000007.12:g.44151189G=	NCBI36
NG_008847.1:g.49359C=
NG_008847.2:g.58106C=

Transcript Alleles

HGVS	Amino-acid change
ENST00000395796.8:c.*1467C=	ENSP00000379142.4:n.*1467C=
ENST00000616242.5:c.*589C=	ENSP00000482149.2:n.*589C=
ENST00000683378.1:n.695C=
ENST00000336642.9:c.*71C=	ENSP00000338009.5:n.*71C=
ENST00000345378.7:c.*71C=	ENSP00000223366.2:n.*71C=
ENST00000403799.8:c.*71C= MANE Select	ENSP00000384247.3:n.*71C=
ENST00000671824.1:c.*71C=	ENSP00000500264.1:n.*71C=
ENST00000672743.1:n.381+100C=
ENST00000673284.1:c.1369+100C=	ENSP00000499852.1:n.1369+100C=
ENST00000336642.8:c.521C=	ENSP00000338009.4:n.521C=
ENST00000345378.6:c.*71C=	ENSP00000223366.2:n.*71C=
ENST00000395796.7:c.*71C=	ENSP00000379142.3:n.*71C=
ENST00000403799.7:c.*71C=	ENSP00000384247.3:n.*71C=
ENST00000459642.1:n.849C=
ENST00000616242.4:c.1466C=	ENSP00000482149.1:n.1466C=
NM_000162.3:c.*71C=	NP_000153.1:n.*71C=
NM_033507.1:c.*71C=	NP_277042.1:n.*71C=
NM_033508.1:c.*71C=	NP_277043.1:n.*71C=
NM_000162.4:c.*71C=	NP_000153.1:n.*71C=
NM_001354800.1:c.1369+100C=	NP_001341729.1:n.1369+100C=
NM_001354801.1:c.*71C=	NP_001341730.1:n.*71C=
NM_001354802.1:c.229+100C=	NP_001341731.1:n.229+100C=
NM_001354803.1:c.*71C=	NP_001341732.1:n.*71C=
NM_033507.2:c.*71C=	NP_277042.1:n.*71C=
NM_033508.2:c.*71C=	NP_277043.1:n.*71C=
XM_024446707.1:c.*71C=	XP_024302475.1:n.*71C=
NM_000162.5:c.*71C= MANE Select	NP_000153.1:n.*71C=
NM_033507.3:c.*71C=	NP_277042.1:n.*71C=
NM_033508.3:c.*71C=	NP_277043.1:n.*71C=
NM_001354803.2:c.*71C=	NP_001341732.1:n.*71C=