Canonical Allele Identifier: CA367396829

Gene: GCK

Linked Data

• MyVariant Identifiers: chr7:g.44184762A>C (hg19) ; chr7:g.44145163A>C (hg38)

Genomic Alleles

HGVS	Genome Assembly
NC_000007.14:g.44145163A>C , CM000669.2:g.44145163A>C	GRCh38
NC_000007.13:g.44184762A>C , CM000669.1:g.44184762A>C	GRCh37
NC_000007.12:g.44151287A>C	NCBI36
NG_008847.1:g.49261T>G
NG_008847.2:g.58008T>G

Transcript Alleles

HGVS	Amino-acid change
ENST00000395796.8:c.*1369T>G	ENSP00000379142.4:n.*1369T>G
ENST00000616242.5:c.*491T>G	ENSP00000482149.2:n.*491T>G
ENST00000683378.1:n.597T>G
ENST00000336642.9:c.405T>G	ENSP00000338009.5:p.Cys135Trp
ENST00000345378.7:c.1374T>G	ENSP00000223366.2:p.Cys458Trp
ENST00000403799.8:c.1371T>G MANE Select	ENSP00000384247.3:p.Cys457Trp
ENST00000671824.1:c.1434T>G	ENSP00000500264.1:p.Cys478Trp
ENST00000672743.1:n.381+2T>G
ENST00000673284.1:c.1369+2T>G	ENSP00000499852.1:n.1369+2T>G
ENST00000336642.8:c.423T>G	ENSP00000338009.4:p.Cys141Trp
ENST00000345378.6:c.1374T>G	ENSP00000223366.2:p.Cys458Trp
ENST00000395796.7:c.1368T>G	ENSP00000379142.3:p.Cys456Trp
ENST00000403799.7:c.1371T>G	ENSP00000384247.3:p.Cys457Trp
ENST00000437084.1:c.1320T>G	ENSP00000402840.1:p.Cys440Trp
ENST00000459642.1:n.751T>G
ENST00000616242.4:c.1368T>G	ENSP00000482149.1:p.Cys456Trp
NM_000162.3:c.1371T>G	NP_000153.1:p.Cys457Trp
NM_033507.1:c.1374T>G	NP_277042.1:p.Cys458Trp
NM_033508.1:c.1368T>G	NP_277043.1:p.Cys456Trp
NM_000162.4:c.1371T>G	NP_000153.1:p.Cys457Trp
NM_001354800.1:c.1369+2T>G	NP_001341729.1:n.1369+2T>G
NM_001354801.1:c.360T>G	NP_001341730.1:p.Cys120Trp
NM_001354802.1:c.229+2T>G	NP_001341731.1:n.229+2T>G
NM_001354803.1:c.405T>G	NP_001341732.1:p.Cys135Trp
NM_033507.2:c.1374T>G	NP_277042.1:p.Cys458Trp
NM_033508.2:c.1368T>G	NP_277043.1:p.Cys456Trp
XM_024446707.1:c.231T>G	XP_024302475.1:p.Cys77Trp
NM_000162.5:c.1371T>G MANE Select	NP_000153.1:p.Cys457Trp
NM_033507.3:c.1374T>G	NP_277042.1:p.Cys458Trp
NM_033508.3:c.1368T>G	NP_277043.1:p.Cys456Trp
NM_001354803.2:c.405T>G	NP_001341732.1:p.Cys135Trp