Canonical Allele Identifier: CA4239649
Gene: GCK HGNC NCBI

Linked Data

dbSNP Id: rs747295070
ExAC: 7:44190714 G / C
gnomAD v2: 7-44190714-G-C
gnomAD v3: 7-44151115-G-C
gnomAD v4: 7-44151115-G-C
MyVariant Identifiers: chr7:g.44190714G>C (hg19) chr7:g.44151115G>C (hg38)
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Genomic Alleles

HGVS Genome Assembly
NC_000007.14:g.44151115G>C , CM000669.2:g.44151115G>C GRCh38
NC_000007.13:g.44190714G>C , CM000669.1:g.44190714G>C GRCh37
NC_000007.12:g.44157239G>C NCBI36
NG_008847.1:g.43309C>G
NG_008847.2:g.52056C>G

Transcript Alleles

HGVS Amino-acid Change
ENST00000395796.8:c.*362-40C>G ENSP00000379142.4:n.*362-40C>G
ENST00000616242.5:c.364-40C>G ENSP00000482149.2:n.364-40C>G
ENST00000682635.1:n.850-40C>G
ENST00000345378.7:c.367-40C>G ENSP00000223366.2:n.367-40C>G
ENST00000403799.8:c.364-40C>G MANE Select ENSP00000384247.3:n.364-40C>G
ENST00000671824.1:c.364-40C>G ENSP00000500264.1:n.364-40C>G
ENST00000673284.1:c.364-40C>G ENSP00000499852.1:n.364-40C>G
ENST00000345378.6:c.367-40C>G ENSP00000223366.2:n.367-40C>G
ENST00000395796.7:c.361-40C>G ENSP00000379142.3:n.361-40C>G
ENST00000403799.7:c.364-40C>G ENSP00000384247.3:n.364-40C>G
ENST00000437084.1:c.364-91C>G ENSP00000402840.1:n.364-91C>G
ENST00000616242.4:c.361-40C>G ENSP00000482149.1:n.361-40C>G
NM_000162.3:c.364-40C>G NP_000153.1:n.364-40C>G
NM_033507.1:c.367-40C>G NP_277042.1:n.367-40C>G
NM_033508.1:c.361-40C>G NP_277043.1:n.361-40C>G
NM_000162.4:c.364-40C>G NP_000153.1:n.364-40C>G
NM_001354800.1:c.364-40C>G NP_001341729.1:n.364-40C>G
NM_033507.2:c.367-40C>G NP_277042.1:n.367-40C>G
NM_033508.2:c.361-40C>G NP_277043.1:n.361-40C>G
NM_000162.5:c.364-40C>G MANE Select NP_000153.1:n.364-40C>G
NM_033507.3:c.367-40C>G NP_277042.1:n.367-40C>G
NM_033508.3:c.361-40C>G NP_277043.1:n.361-40C>G
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