Canonical Allele Identifier: CA2682575651
Gene: GCK HGNC NCBI

Linked Data

gnomAD v4: 7-44151160-T-G
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Genomic Alleles

HGVS Genome Assembly
NC_000007.14:g.44151160T>G , CM000669.2:g.44151160T>G GRCh38
NC_000007.13:g.44190759T>G , CM000669.1:g.44190759T>G GRCh37
NC_000007.12:g.44157284T>G NCBI36
NG_008847.1:g.43264A>C
NG_008847.2:g.52011A>C

Transcript Alleles

HGVS Amino-acid Change
ENST00000395796.8:c.*362-85A>C ENSP00000379142.4:n.*362-85A>C
ENST00000616242.5:c.364-85A>C ENSP00000482149.2:n.364-85A>C
ENST00000682635.1:n.850-85A>C
ENST00000345378.7:c.367-85A>C ENSP00000223366.2:n.367-85A>C
ENST00000403799.8:c.364-85A>C MANE Select ENSP00000384247.3:n.364-85A>C
ENST00000671824.1:c.364-85A>C ENSP00000500264.1:n.364-85A>C
ENST00000673284.1:c.364-85A>C ENSP00000499852.1:n.364-85A>C
ENST00000345378.6:c.367-85A>C ENSP00000223366.2:n.367-85A>C
ENST00000395796.7:c.361-85A>C ENSP00000379142.3:n.361-85A>C
ENST00000403799.7:c.364-85A>C ENSP00000384247.3:n.364-85A>C
ENST00000437084.1:c.364-136A>C ENSP00000402840.1:n.364-136A>C
ENST00000616242.4:c.361-85A>C ENSP00000482149.1:n.361-85A>C
NM_000162.3:c.364-85A>C NP_000153.1:n.364-85A>C
NM_033507.1:c.367-85A>C NP_277042.1:n.367-85A>C
NM_033508.1:c.361-85A>C NP_277043.1:n.361-85A>C
NM_000162.4:c.364-85A>C NP_000153.1:n.364-85A>C
NM_001354800.1:c.364-85A>C NP_001341729.1:n.364-85A>C
NM_033507.2:c.367-85A>C NP_277042.1:n.367-85A>C
NM_033508.2:c.361-85A>C NP_277043.1:n.361-85A>C
NM_000162.5:c.364-85A>C MANE Select NP_000153.1:n.364-85A>C
NM_033507.3:c.367-85A>C NP_277042.1:n.367-85A>C
NM_033508.3:c.361-85A>C NP_277043.1:n.361-85A>C
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