Canonical Allele Identifier: CA1703612644

Gene: GCK

Genomic Alleles

HGVS	Genome Assembly
NC_000007.14:g.44145157C= , CM000669.2:g.44145157C=	GRCh38
NC_000007.13:g.44184756C= , CM000669.1:g.44184756C=	GRCh37
NC_000007.12:g.44151281C=	NCBI36
NG_008847.1:g.49267G=
NG_008847.2:g.58014G=

Transcript Alleles

HGVS	Amino-acid Change
ENST00000395796.8:c.*1375G=	ENSP00000379142.4:n.*1375G=
ENST00000616242.5:c.*497G=	ENSP00000482149.2:n.*497G=
ENST00000683378.1:n.603G=
ENST00000336642.9:c.411G=	ENSP00000338009.5:p.Lys137=
ENST00000345378.7:c.1380G=	ENSP00000223366.2:p.Lys460=
ENST00000403799.8:c.1377G= MANE Select	ENSP00000384247.3:p.Lys459=
ENST00000671824.1:c.1440G=	ENSP00000500264.1:p.Lys480=
ENST00000672743.1:n.381+8G=
ENST00000673284.1:c.1369+8G=	ENSP00000499852.1:n.1369+8G=
ENST00000336642.8:c.429G=	ENSP00000338009.4:p.Lys143=
ENST00000345378.6:c.1380G=	ENSP00000223366.2:p.Lys460=
ENST00000395796.7:c.1374G=	ENSP00000379142.3:p.Lys458=
ENST00000403799.7:c.1377G=	ENSP00000384247.3:p.Lys459=
ENST00000437084.1:c.1326G=	ENSP00000402840.1:p.Lys442=
ENST00000459642.1:n.757G=
ENST00000616242.4:c.1374G=	ENSP00000482149.1:p.Lys458=
NM_000162.3:c.1377G=	NP_000153.1:p.Lys459=
NM_033507.1:c.1380G=	NP_277042.1:p.Lys460=
NM_033508.1:c.1374G=	NP_277043.1:p.Lys458=
NM_000162.4:c.1377G=	NP_000153.1:p.Lys459=
NM_001354800.1:c.1369+8G=	NP_001341729.1:n.1369+8G=
NM_001354801.1:c.366G=	NP_001341730.1:p.Lys122=
NM_001354802.1:c.229+8G=	NP_001341731.1:n.229+8G=
NM_001354803.1:c.411G=	NP_001341732.1:p.Lys137=
NM_033507.2:c.1380G=	NP_277042.1:p.Lys460=
NM_033508.2:c.1374G=	NP_277043.1:p.Lys458=
XM_024446707.1:c.237G=	XP_024302475.1:p.Lys79=
NM_000162.5:c.1377G= MANE Select	NP_000153.1:p.Lys459=
NM_033507.3:c.1380G=	NP_277042.1:p.Lys460=
NM_033508.3:c.1374G=	NP_277043.1:p.Lys458=
NM_001354803.2:c.411G=	NP_001341732.1:p.Lys137=