Canonical Allele Identifier: CA4239564
Gene: GCK HGNC NCBI

Linked Data

ClinVar Variation Id: 911631
dbSNP Id: rs147065275
gnomAD v2: 7-44189389-C-T
gnomAD v3: 7-44149790-C-T
gnomAD v4: 7-44149790-C-T

Genomic Alleles

HGVS Genome Assembly
NC_000007.14:g.44149790C>T , CM000669.2:g.44149790C>T GRCh38
NC_000007.13:g.44189389C>T , CM000669.1:g.44189389C>T GRCh37
NC_000007.12:g.44155914C>T NCBI36
NG_008847.1:g.44634G>A
NG_008847.2:g.53381G>A

Transcript Alleles

HGVS Amino-acid change
ENST00000395796.8:c.*647G>A ENSP00000379142.4:n.*647G>A
ENST00000616242.5:c.649G>A ENSP00000482149.2:p.Asp217Asn
ENST00000682635.1:n.1135G>A
ENST00000345378.7:c.652G>A ENSP00000223366.2:p.Asp218Asn
ENST00000403799.8:c.649G>A MANE Select ENSP00000384247.3:p.Asp217Asn
ENST00000671824.1:c.649G>A ENSP00000500264.1:p.Asp217Asn
ENST00000673284.1:c.649G>A ENSP00000499852.1:p.Asp217Asn
ENST00000345378.6:c.652G>A ENSP00000223366.2:p.Asp218Asn
ENST00000395796.7:c.646G>A ENSP00000379142.3:p.Asp216Asn
ENST00000403799.7:c.649G>A ENSP00000384247.3:p.Asp217Asn
ENST00000437084.1:c.598G>A ENSP00000402840.1:p.Asp200Asn
ENST00000616242.4:c.646G>A ENSP00000482149.1:p.Asp216Asn
NM_000162.3:c.649G>A NP_000153.1:p.Asp217Asn
NM_033507.1:c.652G>A NP_277042.1:p.Asp218Asn
NM_033508.1:c.646G>A NP_277043.1:p.Asp216Asn
NM_000162.4:c.649G>A NP_000153.1:p.Asp217Asn
NM_001354800.1:c.649G>A NP_001341729.1:p.Asp217Asn
NM_033507.2:c.652G>A NP_277042.1:p.Asp218Asn
NM_033508.2:c.646G>A NP_277043.1:p.Asp216Asn
NM_000162.5:c.649G>A MANE Select NP_000153.1:p.Asp217Asn
NM_033507.3:c.652G>A NP_277042.1:p.Asp218Asn
NM_033508.3:c.646G>A NP_277043.1:p.Asp216Asn