Canonical Allele Identifier: CA2682574025
Gene: GCK HGNC NCBI

Linked Data

gnomAD v4: 7-44149938-GCCCCCCCGGCAGGTA-G
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Genomic Alleles

HGVS Genome Assembly
NC_000007.14:g.44149940_44149954del , CM000669.2:g.44149940_44149954del GRCh38
NC_000007.13:g.44189539_44189553del , CM000669.1:g.44189539_44189553del GRCh37
NC_000007.12:g.44156064_44156078del NCBI36
NG_008847.1:g.44471_44485del
NG_008847.2:g.53218_53232del

Transcript Alleles

HGVS Amino-acid Change
ENST00000395796.8:c.*577+16_*577+30del ENSP00000379142.4:n.*577+16_*577+30del
ENST00000616242.5:c.579+16_579+30del ENSP00000482149.2:n.579+16_579+30del
ENST00000682635.1:n.1065+16_1065+30del
ENST00000345378.7:c.582+16_582+30del ENSP00000223366.2:n.582+16_582+30del
ENST00000403799.8:c.579+16_579+30del MANE Select ENSP00000384247.3:n.579+16_579+30del
ENST00000671824.1:c.579+16_579+30del ENSP00000500264.1:n.579+16_579+30del
ENST00000673284.1:c.579+16_579+30del ENSP00000499852.1:n.579+16_579+30del
ENST00000345378.6:c.582+16_582+30del ENSP00000223366.2:n.582+16_582+30del
ENST00000395796.7:c.576+16_576+30del ENSP00000379142.3:n.576+16_576+30del
ENST00000403799.7:c.579+16_579+30del ENSP00000384247.3:n.579+16_579+30del
ENST00000437084.1:c.528+16_528+30del ENSP00000402840.1:n.528+16_528+30del
ENST00000616242.4:c.576+16_576+30del ENSP00000482149.1:n.576+16_576+30del
NM_000162.3:c.579+16_579+30del NP_000153.1:n.579+16_579+30del
NM_033507.1:c.582+16_582+30del NP_277042.1:n.582+16_582+30del
NM_033508.1:c.576+16_576+30del NP_277043.1:n.576+16_576+30del
NM_000162.4:c.579+16_579+30del NP_000153.1:n.579+16_579+30del
NM_001354800.1:c.579+16_579+30del NP_001341729.1:n.579+16_579+30del
NM_033507.2:c.582+16_582+30del NP_277042.1:n.582+16_582+30del
NM_033508.2:c.576+16_576+30del NP_277043.1:n.576+16_576+30del
NM_000162.5:c.579+16_579+30del MANE Select NP_000153.1:n.579+16_579+30del
NM_033507.3:c.582+16_582+30del NP_277042.1:n.582+16_582+30del
NM_033508.3:c.576+16_576+30del NP_277043.1:n.576+16_576+30del
Search 100 bp 5'
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