Canonical Allele Identifier: CA454606338

Gene: GCK

Linked Data

• MyVariant Identifiers: chr7:g.44184759C>T (hg19)

Genomic Alleles

HGVS	Genome Assembly
NC_000007.14:g.44145160C>T , CM000669.2:g.44145160C>T	GRCh38
NC_000007.13:g.44184759C>T , CM000669.1:g.44184759C>T	GRCh37
NC_000007.12:g.44151284C>T	NCBI36
NG_008847.1:g.49264G>A
NG_008847.2:g.58011G>A

Transcript Alleles

HGVS	Amino-acid Change
ENST00000395796.8:c.*1372G>A	ENSP00000379142.4:n.*1372G>A
ENST00000616242.5:c.*494G>A	ENSP00000482149.2:n.*494G>A
ENST00000683378.1:n.600G>A
ENST00000336642.9:c.408G>A	ENSP00000338009.5:p.Lys136=
ENST00000345378.7:c.1377G>A	ENSP00000223366.2:p.Lys459=
ENST00000403799.8:c.1374G>A MANE Select	ENSP00000384247.3:p.Lys458=
ENST00000671824.1:c.1437G>A	ENSP00000500264.1:p.Lys479=
ENST00000672743.1:n.381+5G>A
ENST00000673284.1:c.1369+5G>A	ENSP00000499852.1:n.1369+5G>A
ENST00000336642.8:c.426G>A	ENSP00000338009.4:p.Lys142=
ENST00000345378.6:c.1377G>A	ENSP00000223366.2:p.Lys459=
ENST00000395796.7:c.1371G>A	ENSP00000379142.3:p.Lys457=
ENST00000403799.7:c.1374G>A	ENSP00000384247.3:p.Lys458=
ENST00000437084.1:c.1323G>A	ENSP00000402840.1:p.Lys441=
ENST00000459642.1:n.754G>A
ENST00000616242.4:c.1371G>A	ENSP00000482149.1:p.Lys457=
NM_000162.3:c.1374G>A	NP_000153.1:p.Lys458=
NM_033507.1:c.1377G>A	NP_277042.1:p.Lys459=
NM_033508.1:c.1371G>A	NP_277043.1:p.Lys457=
NM_000162.4:c.1374G>A	NP_000153.1:p.Lys458=
NM_001354800.1:c.1369+5G>A	NP_001341729.1:n.1369+5G>A
NM_001354801.1:c.363G>A	NP_001341730.1:p.Lys121=
NM_001354802.1:c.229+5G>A	NP_001341731.1:n.229+5G>A
NM_001354803.1:c.408G>A	NP_001341732.1:p.Lys136=
NM_033507.2:c.1377G>A	NP_277042.1:p.Lys459=
NM_033508.2:c.1371G>A	NP_277043.1:p.Lys457=
XM_024446707.1:c.234G>A	XP_024302475.1:p.Lys78=
NM_000162.5:c.1374G>A MANE Select	NP_000153.1:p.Lys458=
NM_033507.3:c.1377G>A	NP_277042.1:p.Lys459=
NM_033508.3:c.1371G>A	NP_277043.1:p.Lys457=
NM_001354803.2:c.408G>A	NP_001341732.1:p.Lys136=