Canonical Allele Identifier: CA454609484

Gene: GCK

Linked Data

• MyVariant Identifiers: chr7:g.44189619T>A (hg19)

Genomic Alleles

HGVS	Genome Assembly
NC_000007.14:g.44150020T>A , CM000669.2:g.44150020T>A	GRCh38
NC_000007.13:g.44189619T>A , CM000669.1:g.44189619T>A	GRCh37
NC_000007.12:g.44156144T>A	NCBI36
NG_008847.1:g.44404A>T
NG_008847.2:g.53151A>T

Transcript Alleles

HGVS	Amino-acid Change
ENST00000395796.8:c.*526A>T	ENSP00000379142.4:n.*526A>T
ENST00000616242.5:c.528A>T	ENSP00000482149.2:p.Ala176=
ENST00000682635.1:n.1014A>T
ENST00000345378.7:c.531A>T	ENSP00000223366.2:p.Ala177=
ENST00000403799.8:c.528A>T MANE Select	ENSP00000384247.3:p.Ala176=
ENST00000671824.1:c.528A>T	ENSP00000500264.1:p.Ala176=
ENST00000673284.1:c.528A>T	ENSP00000499852.1:p.Ala176=
ENST00000345378.6:c.531A>T	ENSP00000223366.2:p.Ala177=
ENST00000395796.7:c.525A>T	ENSP00000379142.3:p.Ala175=
ENST00000403799.7:c.528A>T	ENSP00000384247.3:p.Ala176=
ENST00000437084.1:c.477A>T	ENSP00000402840.1:p.Ala159=
ENST00000616242.4:c.525A>T	ENSP00000482149.1:p.Ala175=
NM_000162.3:c.528A>T	NP_000153.1:p.Ala176=
NM_033507.1:c.531A>T	NP_277042.1:p.Ala177=
NM_033508.1:c.525A>T	NP_277043.1:p.Ala175=
NM_000162.4:c.528A>T	NP_000153.1:p.Ala176=
NM_001354800.1:c.528A>T	NP_001341729.1:p.Ala176=
NM_033507.2:c.531A>T	NP_277042.1:p.Ala177=
NM_033508.2:c.525A>T	NP_277043.1:p.Ala175=
NM_000162.5:c.528A>T MANE Select	NP_000153.1:p.Ala176=
NM_033507.3:c.531A>T	NP_277042.1:p.Ala177=
NM_033508.3:c.525A>T	NP_277043.1:p.Ala175=