Canonical Allele Identifier: CA2682578767
Gene: GCK HGNC NCBI

Linked Data

gnomAD v4: 7-44144778-A-C
JSON-LD

Genomic Alleles

HGVS Genome Assembly
NC_000007.14:g.44144778A>C , CM000669.2:g.44144778A>C GRCh38
NC_000007.13:g.44184377A>C , CM000669.1:g.44184377A>C GRCh37
NC_000007.12:g.44150902A>C NCBI36
NG_008847.1:g.49646T>G
NG_008847.2:g.58393T>G

Transcript Alleles

HGVS Amino-acid Change
ENST00000395796.8:c.*1754T>G ENSP00000379142.4:n.*1754T>G
ENST00000616242.5:c.*876T>G ENSP00000482149.2:n.*876T>G
ENST00000683378.1:n.982T>G
ENST00000336642.9:c.*358T>G ENSP00000338009.5:n.*358T>G
ENST00000345378.7:c.*358T>G ENSP00000223366.2:n.*358T>G
ENST00000403799.8:c.*358T>G MANE Select ENSP00000384247.3:n.*358T>G
ENST00000671824.1:c.*358T>G ENSP00000500264.1:n.*358T>G
ENST00000672743.1:n.381+387T>G
ENST00000673284.1:c.1369+387T>G ENSP00000499852.1:n.1369+387T>G
ENST00000336642.8:c.808T>G ENSP00000338009.4:n.808T>G
ENST00000345378.6:c.*358T>G ENSP00000223366.2:n.*358T>G
ENST00000395796.7:c.*358T>G ENSP00000379142.3:n.*358T>G
ENST00000403799.7:c.*358T>G ENSP00000384247.3:n.*358T>G
ENST00000459642.1:n.1136T>G
ENST00000616242.4:c.1753T>G ENSP00000482149.1:n.1753T>G
NM_000162.3:c.*358T>G NP_000153.1:n.*358T>G
NM_033507.1:c.*358T>G NP_277042.1:n.*358T>G
NM_033508.1:c.*358T>G NP_277043.1:n.*358T>G
NM_000162.4:c.*358T>G NP_000153.1:n.*358T>G
NM_001354800.1:c.1369+387T>G NP_001341729.1:n.1369+387T>G
NM_001354801.1:c.*358T>G NP_001341730.1:n.*358T>G
NM_001354802.1:c.229+387T>G NP_001341731.1:n.229+387T>G
NM_001354803.1:c.*358T>G NP_001341732.1:n.*358T>G
NM_033507.2:c.*358T>G NP_277042.1:n.*358T>G
NM_033508.2:c.*358T>G NP_277043.1:n.*358T>G
XM_024446707.1:c.*358T>G XP_024302475.1:n.*358T>G
NM_000162.5:c.*358T>G MANE Select NP_000153.1:n.*358T>G
NM_033507.3:c.*358T>G NP_277042.1:n.*358T>G
NM_033508.3:c.*358T>G NP_277043.1:n.*358T>G
NM_001354803.2:c.*358T>G NP_001341732.1:n.*358T>G
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