Canonical Allele Identifier: CA367401512
Gene: GCK HGNC NCBI

Linked Data

MyVariant Identifiers: chr7:g.44189570C>A (hg19) chr7:g.44149971C>A (hg38)
JSON-LD

Genomic Alleles

HGVS Genome Assembly
NC_000007.14:g.44149971C>A , CM000669.2:g.44149971C>A GRCh38
NC_000007.13:g.44189570C>A , CM000669.1:g.44189570C>A GRCh37
NC_000007.12:g.44156095C>A NCBI36
NG_008847.1:g.44453G>T
NG_008847.2:g.53200G>T

Transcript Alleles

HGVS Amino-acid Change
ENST00000395796.8:c.*575G>T ENSP00000379142.4:n.*575G>T
ENST00000616242.5:c.577G>T ENSP00000482149.2:p.Gly193Trp
ENST00000682635.1:n.1063G>T
ENST00000345378.7:c.580G>T ENSP00000223366.2:p.Gly194Trp
ENST00000403799.8:c.577G>T MANE Select ENSP00000384247.3:p.Gly193Trp
ENST00000671824.1:c.577G>T ENSP00000500264.1:p.Gly193Trp
ENST00000673284.1:c.577G>T ENSP00000499852.1:p.Gly193Trp
ENST00000345378.6:c.580G>T ENSP00000223366.2:p.Gly194Trp
ENST00000395796.7:c.574G>T ENSP00000379142.3:p.Gly192Trp
ENST00000403799.7:c.577G>T ENSP00000384247.3:p.Gly193Trp
ENST00000437084.1:c.526G>T ENSP00000402840.1:p.Gly176Trp
ENST00000616242.4:c.574G>T ENSP00000482149.1:p.Gly192Trp
NM_000162.3:c.577G>T NP_000153.1:p.Gly193Trp
NM_033507.1:c.580G>T NP_277042.1:p.Gly194Trp
NM_033508.1:c.574G>T NP_277043.1:p.Gly192Trp
NM_000162.4:c.577G>T NP_000153.1:p.Gly193Trp
NM_001354800.1:c.577G>T NP_001341729.1:p.Gly193Trp
NM_033507.2:c.580G>T NP_277042.1:p.Gly194Trp
NM_033508.2:c.574G>T NP_277043.1:p.Gly192Trp
NM_000162.5:c.577G>T MANE Select NP_000153.1:p.Gly193Trp
NM_033507.3:c.580G>T NP_277042.1:p.Gly194Trp
NM_033508.3:c.574G>T NP_277043.1:p.Gly192Trp
Search 100 bp 5'
Search 100 bp 3'