Canonical Allele Identifier: CA1703612942

Gene: GCK

Genomic Alleles

HGVS	Genome Assembly
NC_000007.14:g.44145651C= , CM000669.2:g.44145651C=	GRCh38
NC_000007.13:g.44185250C= , CM000669.1:g.44185250C=	GRCh37
NC_000007.12:g.44151775C=	NCBI36
NG_008847.1:g.48773G=
NG_008847.2:g.57520G=

Transcript Alleles

HGVS	Amino-acid Change
ENST00000395796.8:c.*1097G=	ENSP00000379142.4:n.*1097G=
ENST00000616242.5:c.*219G=	ENSP00000482149.2:n.*219G=
ENST00000683378.1:n.325G=
ENST00000336642.9:c.133G=	ENSP00000338009.5:p.Val45=
ENST00000345378.7:c.1102G=	ENSP00000223366.2:p.Val368=
ENST00000403799.8:c.1099G= MANE Select	ENSP00000384247.3:p.Val367=
ENST00000671824.1:c.1162G=	ENSP00000500264.1:p.Val388=
ENST00000672743.1:n.111G=
ENST00000673284.1:c.1099G=	ENSP00000499852.1:p.Val367=
ENST00000336642.8:c.151G=	ENSP00000338009.4:p.Val51=
ENST00000345378.6:c.1102G=	ENSP00000223366.2:p.Val368=
ENST00000395796.7:c.1096G=	ENSP00000379142.3:p.Val366=
ENST00000403799.7:c.1099G=	ENSP00000384247.3:p.Val367=
ENST00000437084.1:c.1048G=	ENSP00000402840.1:p.Val350=
ENST00000459642.1:n.479G=
ENST00000473353.1:n.397G=
ENST00000616242.4:c.1096G=	ENSP00000482149.1:p.Val366=
NM_000162.3:c.1099G=	NP_000153.1:p.Val367=
NM_033507.1:c.1102G=	NP_277042.1:p.Val368=
NM_033508.1:c.1096G=	NP_277043.1:p.Val366=
NM_000162.4:c.1099G=	NP_000153.1:p.Val367=
NM_001354800.1:c.1099G=	NP_001341729.1:p.Val367=
NM_001354801.1:c.88G=	NP_001341730.1:p.Val30=
NM_001354802.1:c.-42G=	NP_001341731.1:n.-42G=
NM_001354803.1:c.133G=	NP_001341732.1:p.Val45=
NM_033507.2:c.1102G=	NP_277042.1:p.Val368=
NM_033508.2:c.1096G=	NP_277043.1:p.Val366=
XM_024446707.1:c.-42G=	XP_024302475.1:n.-42G=
NM_000162.5:c.1099G= MANE Select	NP_000153.1:p.Val367=
NM_033507.3:c.1102G=	NP_277042.1:p.Val368=
NM_033508.3:c.1096G=	NP_277043.1:p.Val366=
NM_001354803.2:c.133G=	NP_001341732.1:p.Val45=