Canonical Allele Identifier: CA2682574962
Gene: GCK HGNC NCBI

Linked Data

gnomAD v4: 7-44189383-T-C
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Genomic Alleles

HGVS Genome Assembly
NC_000007.14:g.44189383T>C , CM000669.2:g.44189383T>C GRCh38
NC_000007.13:g.44228982T>C , CM000669.1:g.44228982T>C GRCh37
NC_000007.12:g.44195507T>C NCBI36
NG_008847.1:g.5041A>G
NG_008847.2:g.13788A>G

Transcript Alleles

HGVS Amino-acid change
ENST00000616242.5:c.-430A>G ENSP00000482149.2:n.-430A>G
ENST00000682635.1:n.57A>G
ENST00000403799.8:c.-430A>G MANE Select ENSP00000384247.3:n.-430A>G
ENST00000671824.1:c.-430A>G ENSP00000500264.1:n.-430A>G
ENST00000673284.1:c.-430A>G ENSP00000499852.1:n.-430A>G
ENST00000403799.7:c.-430A>G ENSP00000384247.3:n.-430A>G
ENST00000476008.1:n.480+8308A>G
NM_000162.3:c.-430A>G NP_000153.1:n.-430A>G
NM_000162.4:c.-430A>G NP_000153.1:n.-430A>G
NM_001354800.1:c.-430A>G NP_001341729.1:n.-430A>G
NM_000162.5:c.-430A>G MANE Select NP_000153.1:n.-430A>G
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