Canonical Allele Identifier: CA1703612694

Gene: GCK

Genomic Alleles

HGVS	Genome Assembly
NC_000007.14:g.44145245A= , CM000669.2:g.44145245A=	GRCh38
NC_000007.13:g.44184844A= , CM000669.1:g.44184844A=	GRCh37
NC_000007.12:g.44151369A=	NCBI36
NG_008847.1:g.49179T=
NG_008847.2:g.57926T=

Transcript Alleles

HGVS	Amino-acid Change
ENST00000395796.8:c.*1287T=	ENSP00000379142.4:n.*1287T=
ENST00000616242.5:c.*409T=	ENSP00000482149.2:n.*409T=
ENST00000683378.1:n.515T=
ENST00000336642.9:c.323T=	ENSP00000338009.5:p.Leu108=
ENST00000345378.7:c.1292T=	ENSP00000223366.2:p.Leu431=
ENST00000403799.8:c.1289T= MANE Select	ENSP00000384247.3:p.Leu430=
ENST00000671824.1:c.1352T=	ENSP00000500264.1:p.Leu451=
ENST00000672743.1:n.301T=
ENST00000673284.1:c.1289T=	ENSP00000499852.1:p.Leu430=
ENST00000336642.8:c.341T=	ENSP00000338009.4:p.Leu114=
ENST00000345378.6:c.1292T=	ENSP00000223366.2:p.Leu431=
ENST00000395796.7:c.1286T=	ENSP00000379142.3:p.Leu429=
ENST00000403799.7:c.1289T=	ENSP00000384247.3:p.Leu430=
ENST00000437084.1:c.1238T=	ENSP00000402840.1:p.Leu413=
ENST00000459642.1:n.669T=
ENST00000616242.4:c.1286T=	ENSP00000482149.1:p.Leu429=
NM_000162.3:c.1289T=	NP_000153.1:p.Leu430=
NM_033507.1:c.1292T=	NP_277042.1:p.Leu431=
NM_033508.1:c.1286T=	NP_277043.1:p.Leu429=
NM_000162.4:c.1289T=	NP_000153.1:p.Leu430=
NM_001354800.1:c.1289T=	NP_001341729.1:p.Leu430=
NM_001354801.1:c.278T=	NP_001341730.1:p.Leu93=
NM_001354802.1:c.149T=	NP_001341731.1:p.Leu50=
NM_001354803.1:c.323T=	NP_001341732.1:p.Leu108=
NM_033507.2:c.1292T=	NP_277042.1:p.Leu431=
NM_033508.2:c.1286T=	NP_277043.1:p.Leu429=
XM_024446707.1:c.149T=	XP_024302475.1:p.Leu50=
NM_000162.5:c.1289T= MANE Select	NP_000153.1:p.Leu430=
NM_033507.3:c.1292T=	NP_277042.1:p.Leu431=
NM_033508.3:c.1286T=	NP_277043.1:p.Leu429=
NM_001354803.2:c.323T=	NP_001341732.1:p.Leu108=