Canonical Allele Identifier: CA454608963
Gene: GCK HGNC NCBI

Linked Data

MyVariant Identifiers: chr7:g.44189360C>G (hg19)

Genomic Alleles

HGVS Genome Assembly
NC_000007.14:g.44149761C>G , CM000669.2:g.44149761C>G GRCh38
NC_000007.13:g.44189360C>G , CM000669.1:g.44189360C>G GRCh37
NC_000007.12:g.44155885C>G NCBI36
NG_008847.1:g.44663G>C
NG_008847.2:g.53410G>C

Transcript Alleles

HGVS Amino-acid change
ENST00000395796.8:c.*676G>C ENSP00000379142.4:n.*676G>C
ENST00000616242.5:c.678G>C ENSP00000482149.2:p.Val226=
ENST00000682635.1:n.1164G>C
ENST00000345378.7:c.681G>C ENSP00000223366.2:p.Val227=
ENST00000403799.8:c.678G>C MANE Select ENSP00000384247.3:p.Val226=
ENST00000671824.1:c.678G>C ENSP00000500264.1:p.Val226=
ENST00000673284.1:c.678G>C ENSP00000499852.1:p.Val226=
ENST00000345378.6:c.681G>C ENSP00000223366.2:p.Val227=
ENST00000395796.7:c.675G>C ENSP00000379142.3:p.Val225=
ENST00000403799.7:c.678G>C ENSP00000384247.3:p.Val226=
ENST00000437084.1:c.627G>C ENSP00000402840.1:p.Val209=
ENST00000616242.4:c.675G>C ENSP00000482149.1:p.Val225=
NM_000162.3:c.678G>C NP_000153.1:p.Val226=
NM_033507.1:c.681G>C NP_277042.1:p.Val227=
NM_033508.1:c.675G>C NP_277043.1:p.Val225=
XR_927223.1:n.276C>G
NM_000162.4:c.678G>C NP_000153.1:p.Val226=
NM_001354800.1:c.678G>C NP_001341729.1:p.Val226=
NM_033507.2:c.681G>C NP_277042.1:p.Val227=
NM_033508.2:c.675G>C NP_277043.1:p.Val225=
XR_927223.2:n.276C>G
NM_000162.5:c.678G>C MANE Select NP_000153.1:p.Val226=
NM_033507.3:c.681G>C NP_277042.1:p.Val227=
NM_033508.3:c.675G>C NP_277043.1:p.Val225=