Canonical Allele Identifier: CA367400703
Gene: GCK HGNC NCBI

Linked Data

ClinVar Variation Id: 2136514
ClinVar RCV Id: RCV003037216
MyVariant Identifiers: chr7:g.44187393T>G (hg19) chr7:g.44147794T>G (hg38)
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Genomic Alleles

HGVS Genome Assembly
NC_000007.14:g.44147794T>G , CM000669.2:g.44147794T>G GRCh38
NC_000007.13:g.44187393T>G , CM000669.1:g.44187393T>G GRCh37
NC_000007.12:g.44153918T>G NCBI36
NG_008847.1:g.46630A>C
NG_008847.2:g.55377A>C

Transcript Alleles

HGVS Amino-acid Change
ENST00000395796.8:c.*717A>C ENSP00000379142.4:n.*717A>C
ENST00000616242.5:c.719A>C ENSP00000482149.2:p.Asn240Thr
ENST00000345378.7:c.722A>C ENSP00000223366.2:p.Asn241Thr
ENST00000403799.8:c.719A>C MANE Select ENSP00000384247.3:p.Asn240Thr
ENST00000671824.1:c.719A>C ENSP00000500264.1:p.Asn240Thr
ENST00000673284.1:c.719A>C ENSP00000499852.1:p.Asn240Thr
ENST00000345378.6:c.722A>C ENSP00000223366.2:p.Asn241Thr
ENST00000395796.7:c.716A>C ENSP00000379142.3:p.Asn239Thr
ENST00000403799.7:c.719A>C ENSP00000384247.3:p.Asn240Thr
ENST00000437084.1:c.668A>C ENSP00000402840.1:p.Asn223Thr
ENST00000616242.4:c.716A>C ENSP00000482149.1:p.Asn239Thr
NM_000162.3:c.719A>C NP_000153.1:p.Asn240Thr
NM_033507.1:c.722A>C NP_277042.1:p.Asn241Thr
NM_033508.1:c.716A>C NP_277043.1:p.Asn239Thr
XR_927223.1:n.82+46T>G
NM_000162.4:c.719A>C NP_000153.1:p.Asn240Thr
NM_001354800.1:c.719A>C NP_001341729.1:p.Asn240Thr
NM_033507.2:c.722A>C NP_277042.1:p.Asn241Thr
NM_033508.2:c.716A>C NP_277043.1:p.Asn239Thr
XR_927223.2:n.82+46T>G
NM_000162.5:c.719A>C MANE Select NP_000153.1:p.Asn240Thr
NM_033507.3:c.722A>C NP_277042.1:p.Asn241Thr
NM_033508.3:c.716A>C NP_277043.1:p.Asn239Thr
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