Canonical Allele Identifier: CA454606344

Gene: GCK

Linked Data

• MyVariant Identifiers: chr7:g.44184768C>G (hg19)

Genomic Alleles

HGVS	Genome Assembly
NC_000007.14:g.44145169C>G , CM000669.2:g.44145169C>G	GRCh38
NC_000007.13:g.44184768C>G , CM000669.1:g.44184768C>G	GRCh37
NC_000007.12:g.44151293C>G	NCBI36
NG_008847.1:g.49255G>C
NG_008847.2:g.58002G>C

Transcript Alleles

HGVS	Amino-acid change
ENST00000395796.8:c.*1363G>C	ENSP00000379142.4:n.*1363G>C
ENST00000616242.5:c.*485G>C	ENSP00000482149.2:n.*485G>C
ENST00000683378.1:n.591G>C
ENST00000336642.9:c.399G>C	ENSP00000338009.5:p.Val133=
ENST00000345378.7:c.1368G>C	ENSP00000223366.2:p.Val456=
ENST00000403799.8:c.1365G>C MANE Select	ENSP00000384247.3:p.Val455=
ENST00000671824.1:c.1428G>C	ENSP00000500264.1:p.Val476=
ENST00000672743.1:n.377G>C
ENST00000673284.1:c.1365G>C	ENSP00000499852.1:p.Val455=
ENST00000336642.8:c.417G>C	ENSP00000338009.4:p.Val139=
ENST00000345378.6:c.1368G>C	ENSP00000223366.2:p.Val456=
ENST00000395796.7:c.1362G>C	ENSP00000379142.3:p.Val454=
ENST00000403799.7:c.1365G>C	ENSP00000384247.3:p.Val455=
ENST00000437084.1:c.1314G>C	ENSP00000402840.1:p.Val438=
ENST00000459642.1:n.745G>C
ENST00000616242.4:c.1362G>C	ENSP00000482149.1:p.Val454=
NM_000162.3:c.1365G>C	NP_000153.1:p.Val455=
NM_033507.1:c.1368G>C	NP_277042.1:p.Val456=
NM_033508.1:c.1362G>C	NP_277043.1:p.Val454=
NM_000162.4:c.1365G>C	NP_000153.1:p.Val455=
NM_001354800.1:c.1365G>C	NP_001341729.1:p.Val455=
NM_001354801.1:c.354G>C	NP_001341730.1:p.Val118=
NM_001354802.1:c.225G>C	NP_001341731.1:p.Val75=
NM_001354803.1:c.399G>C	NP_001341732.1:p.Val133=
NM_033507.2:c.1368G>C	NP_277042.1:p.Val456=
NM_033508.2:c.1362G>C	NP_277043.1:p.Val454=
XM_024446707.1:c.225G>C	XP_024302475.1:p.Val75=
NM_000162.5:c.1365G>C MANE Select	NP_000153.1:p.Val455=
NM_033507.3:c.1368G>C	NP_277042.1:p.Val456=
NM_033508.3:c.1362G>C	NP_277043.1:p.Val454=
NM_001354803.2:c.399G>C	NP_001341732.1:p.Val133=