Canonical Allele Identifier: CA454863158

Gene: GCK

Linked Data

• MyVariant Identifiers: chr7:g.44185146T>C (hg19)

Genomic Alleles

HGVS	Genome Assembly
NC_000007.14:g.44145547T>C , CM000669.2:g.44145547T>C	GRCh38
NC_000007.13:g.44185146T>C , CM000669.1:g.44185146T>C	GRCh37
NC_000007.12:g.44151671T>C	NCBI36
NG_008847.1:g.48877A>G
NG_008847.2:g.57624A>G

Transcript Alleles

HGVS	Amino-acid change
ENST00000395796.8:c.*1201A>G	ENSP00000379142.4:n.*1201A>G
ENST00000616242.5:c.*323A>G	ENSP00000482149.2:n.*323A>G
ENST00000683378.1:n.429A>G
ENST00000336642.9:c.237A>G	ENSP00000338009.5:p.Val79=
ENST00000345378.7:c.1206A>G	ENSP00000223366.2:p.Val402=
ENST00000403799.8:c.1203A>G MANE Select	ENSP00000384247.3:p.Val401=
ENST00000671824.1:c.1266A>G	ENSP00000500264.1:p.Val422=
ENST00000672743.1:n.215A>G
ENST00000673284.1:c.1203A>G	ENSP00000499852.1:p.Val401=
ENST00000336642.8:c.255A>G	ENSP00000338009.4:p.Val85=
ENST00000345378.6:c.1206A>G	ENSP00000223366.2:p.Val402=
ENST00000395796.7:c.1200A>G	ENSP00000379142.3:p.Val400=
ENST00000403799.7:c.1203A>G	ENSP00000384247.3:p.Val401=
ENST00000437084.1:c.1152A>G	ENSP00000402840.1:p.Val384=
ENST00000459642.1:n.583A>G
ENST00000616242.4:c.1200A>G	ENSP00000482149.1:p.Val400=
NM_000162.3:c.1203A>G	NP_000153.1:p.Val401=
NM_033507.1:c.1206A>G	NP_277042.1:p.Val402=
NM_033508.1:c.1200A>G	NP_277043.1:p.Val400=
NM_000162.4:c.1203A>G	NP_000153.1:p.Val401=
NM_001354800.1:c.1203A>G	NP_001341729.1:p.Val401=
NM_001354801.1:c.192A>G	NP_001341730.1:p.Val64=
NM_001354802.1:c.63A>G	NP_001341731.1:p.Val21=
NM_001354803.1:c.237A>G	NP_001341732.1:p.Val79=
NM_033507.2:c.1206A>G	NP_277042.1:p.Val402=
NM_033508.2:c.1200A>G	NP_277043.1:p.Val400=
XM_024446707.1:c.63A>G	XP_024302475.1:p.Val21=
NM_000162.5:c.1203A>G MANE Select	NP_000153.1:p.Val401=
NM_033507.3:c.1206A>G	NP_277042.1:p.Val402=
NM_033508.3:c.1200A>G	NP_277043.1:p.Val400=
NM_001354803.2:c.237A>G	NP_001341732.1:p.Val79=