Canonical Allele Identifier: CA1100760774
Gene: GCK HGNC NCBI

Linked Data

dbSNP Id: rs2096280315
gnomAD v3: 7-44151116-G-GT
gnomAD v4: 7-44151116-G-GT
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Genomic Alleles

HGVS Genome Assembly
NC_000007.14:g.44151117dup , CM000669.2:g.44151117dup GRCh38
NC_000007.13:g.44190716dup , CM000669.1:g.44190716dup GRCh37
NC_000007.12:g.44157241dup NCBI36
NG_008847.1:g.43307dup
NG_008847.2:g.52054dup

Transcript Alleles

HGVS Amino-acid Change
ENST00000395796.8:c.*362-42dup ENSP00000379142.4:n.*362-42dup
ENST00000616242.5:c.364-42dup ENSP00000482149.2:n.364-42dup
ENST00000682635.1:n.850-42dup
ENST00000345378.7:c.367-42dup ENSP00000223366.2:n.367-42dup
ENST00000403799.8:c.364-42dup MANE Select ENSP00000384247.3:n.364-42dup
ENST00000671824.1:c.364-42dup ENSP00000500264.1:n.364-42dup
ENST00000673284.1:c.364-42dup ENSP00000499852.1:n.364-42dup
ENST00000345378.6:c.367-42dup ENSP00000223366.2:n.367-42dup
ENST00000395796.7:c.361-42dup ENSP00000379142.3:n.361-42dup
ENST00000403799.7:c.364-42dup ENSP00000384247.3:n.364-42dup
ENST00000437084.1:c.364-93dup ENSP00000402840.1:n.364-93dup
ENST00000616242.4:c.361-42dup ENSP00000482149.1:n.361-42dup
NM_000162.3:c.364-42dup NP_000153.1:n.364-42dup
NM_033507.1:c.367-42dup NP_277042.1:n.367-42dup
NM_033508.1:c.361-42dup NP_277043.1:n.361-42dup
NM_000162.4:c.364-42dup NP_000153.1:n.364-42dup
NM_001354800.1:c.364-42dup NP_001341729.1:n.364-42dup
NM_033507.2:c.367-42dup NP_277042.1:n.367-42dup
NM_033508.2:c.361-42dup NP_277043.1:n.361-42dup
NM_000162.5:c.364-42dup MANE Select NP_000153.1:n.364-42dup
NM_033507.3:c.367-42dup NP_277042.1:n.367-42dup
NM_033508.3:c.361-42dup NP_277043.1:n.361-42dup
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