Canonical Allele Identifier: CA367401149
Gene: GCK HGNC NCBI

Linked Data

ClinVar Variation Id: 1464253
dbSNP Id: rs2128821476

Genomic Alleles

HGVS Genome Assembly
NC_000007.14:g.44149768A>G , CM000669.2:g.44149768A>G GRCh38
NC_000007.13:g.44189367A>G , CM000669.1:g.44189367A>G GRCh37
NC_000007.12:g.44155892A>G NCBI36
NG_008847.1:g.44656T>C
NG_008847.2:g.53403T>C

Transcript Alleles

HGVS Amino-acid Change
ENST00000395796.8:c.*669T>C ENSP00000379142.4:n.*669T>C
ENST00000616242.5:c.671T>C ENSP00000482149.2:p.Met224Thr
ENST00000682635.1:n.1157T>C
ENST00000345378.7:c.674T>C ENSP00000223366.2:p.Met225Thr
ENST00000403799.8:c.671T>C MANE Select ENSP00000384247.3:p.Met224Thr
ENST00000671824.1:c.671T>C ENSP00000500264.1:p.Met224Thr
ENST00000673284.1:c.671T>C ENSP00000499852.1:p.Met224Thr
ENST00000345378.6:c.674T>C ENSP00000223366.2:p.Met225Thr
ENST00000395796.7:c.668T>C ENSP00000379142.3:p.Met223Thr
ENST00000403799.7:c.671T>C ENSP00000384247.3:p.Met224Thr
ENST00000437084.1:c.620T>C ENSP00000402840.1:p.Met207Thr
ENST00000616242.4:c.668T>C ENSP00000482149.1:p.Met223Thr
NM_000162.3:c.671T>C NP_000153.1:p.Met224Thr
NM_033507.1:c.674T>C NP_277042.1:p.Met225Thr
NM_033508.1:c.668T>C NP_277043.1:p.Met223Thr
XR_927223.1:n.283A>G
NM_000162.4:c.671T>C NP_000153.1:p.Met224Thr
NM_001354800.1:c.671T>C NP_001341729.1:p.Met224Thr
NM_033507.2:c.674T>C NP_277042.1:p.Met225Thr
NM_033508.2:c.668T>C NP_277043.1:p.Met223Thr
XR_927223.2:n.283A>G
NM_000162.5:c.671T>C MANE Select NP_000153.1:p.Met224Thr
NM_033507.3:c.674T>C NP_277042.1:p.Met225Thr
NM_033508.3:c.668T>C NP_277043.1:p.Met223Thr