Canonical Allele Identifier: CA454609141
Gene: GCK HGNC NCBI

Linked Data

MyVariant Identifiers: chr7:g.44189435T>A (hg19)

Genomic Alleles

HGVS Genome Assembly
NC_000007.14:g.44149836T>A , CM000669.2:g.44149836T>A GRCh38
NC_000007.13:g.44189435T>A , CM000669.1:g.44189435T>A GRCh37
NC_000007.12:g.44155960T>A NCBI36
NG_008847.1:g.44588A>T
NG_008847.2:g.53335A>T

Transcript Alleles

HGVS Amino-acid change
ENST00000395796.8:c.*601A>T ENSP00000379142.4:n.*601A>T
ENST00000616242.5:c.603A>T ENSP00000482149.2:p.Ala201=
ENST00000682635.1:n.1089A>T
ENST00000345378.7:c.606A>T ENSP00000223366.2:p.Ala202=
ENST00000403799.8:c.603A>T MANE Select ENSP00000384247.3:p.Ala201=
ENST00000671824.1:c.603A>T ENSP00000500264.1:p.Ala201=
ENST00000673284.1:c.603A>T ENSP00000499852.1:p.Ala201=
ENST00000345378.6:c.606A>T ENSP00000223366.2:p.Ala202=
ENST00000395796.7:c.600A>T ENSP00000379142.3:p.Ala200=
ENST00000403799.7:c.603A>T ENSP00000384247.3:p.Ala201=
ENST00000437084.1:c.552A>T ENSP00000402840.1:p.Ala184=
ENST00000616242.4:n.600A>T ENSP00000482149.1:p.Ala200=
NM_000162.3:c.603A>T NP_000153.1:p.Ala201=
NM_033507.1:c.606A>T NP_277042.1:p.Ala202=
NM_033508.1:c.600A>T NP_277043.1:p.Ala200=
NM_000162.4:c.603A>T NP_000153.1:p.Ala201=
NM_001354800.1:c.603A>T NP_001341729.1:p.Ala201=
NM_033507.2:c.606A>T NP_277042.1:p.Ala202=
NM_033508.2:c.600A>T NP_277043.1:p.Ala200=
NM_000162.5:c.603A>T MANE Select NP_000153.1:p.Ala201=
NM_033507.3:c.606A>T NP_277042.1:p.Ala202=
NM_033508.3:c.600A>T NP_277043.1:p.Ala200=