Canonical Allele Identifier: CA454606329

Gene: GCK

Linked Data

• gnomAD v4: 7-44145142-G-T
• MyVariant Identifiers: chr7:g.44184741G>T (hg19)

Genomic Alleles

HGVS	Genome Assembly
NC_000007.14:g.44145142G>T , CM000669.2:g.44145142G>T	GRCh38
NC_000007.13:g.44184741G>T , CM000669.1:g.44184741G>T	GRCh37
NC_000007.12:g.44151266G>T	NCBI36
NG_008847.1:g.49282C>A
NG_008847.2:g.58029C>A

Transcript Alleles

HGVS	Amino-acid Change
ENST00000395796.8:c.*1390C>A	ENSP00000379142.4:n.*1390C>A
ENST00000616242.5:c.*512C>A	ENSP00000482149.2:n.*512C>A
ENST00000683378.1:n.618C>A
ENST00000336642.9:c.426C>A	ENSP00000338009.5:p.Gly142=
ENST00000345378.7:c.1395C>A	ENSP00000223366.2:p.Gly465=
ENST00000403799.8:c.1392C>A MANE Select	ENSP00000384247.3:p.Gly464=
ENST00000671824.1:c.1455C>A	ENSP00000500264.1:p.Gly485=
ENST00000672743.1:n.381+23C>A
ENST00000673284.1:c.1369+23C>A	ENSP00000499852.1:n.1369+23C>A
ENST00000336642.8:c.444C>A	ENSP00000338009.4:p.Gly148=
ENST00000345378.6:c.1395C>A	ENSP00000223366.2:p.Gly465=
ENST00000395796.7:c.1389C>A	ENSP00000379142.3:p.Gly463=
ENST00000403799.7:c.1392C>A	ENSP00000384247.3:p.Gly464=
ENST00000437084.1:c.1341C>A	ENSP00000402840.1:p.Gly447=
ENST00000459642.1:n.772C>A
ENST00000616242.4:c.1389C>A	ENSP00000482149.1:p.Gly463=
NM_000162.3:c.1392C>A	NP_000153.1:p.Gly464=
NM_033507.1:c.1395C>A	NP_277042.1:p.Gly465=
NM_033508.1:c.1389C>A	NP_277043.1:p.Gly463=
NM_000162.4:c.1392C>A	NP_000153.1:p.Gly464=
NM_001354800.1:c.1369+23C>A	NP_001341729.1:n.1369+23C>A
NM_001354801.1:c.381C>A	NP_001341730.1:p.Gly127=
NM_001354802.1:c.229+23C>A	NP_001341731.1:n.229+23C>A
NM_001354803.1:c.426C>A	NP_001341732.1:p.Gly142=
NM_033507.2:c.1395C>A	NP_277042.1:p.Gly465=
NM_033508.2:c.1389C>A	NP_277043.1:p.Gly463=
XM_024446707.1:c.252C>A	XP_024302475.1:p.Gly84=
NM_000162.5:c.1392C>A MANE Select	NP_000153.1:p.Gly464=
NM_033507.3:c.1395C>A	NP_277042.1:p.Gly465=
NM_033508.3:c.1389C>A	NP_277043.1:p.Gly463=
NM_001354803.2:c.426C>A	NP_001341732.1:p.Gly142=