Canonical Allele Identifier: CA2682574946
Gene: GCK HGNC NCBI

Linked Data

gnomAD v4: 7-44189379-A-C
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Genomic Alleles

HGVS Genome Assembly
NC_000007.14:g.44189379A>C , CM000669.2:g.44189379A>C GRCh38
NC_000007.13:g.44228978A>C , CM000669.1:g.44228978A>C GRCh37
NC_000007.12:g.44195503A>C NCBI36
NG_008847.1:g.5045T>G
NG_008847.2:g.13792T>G

Transcript Alleles

HGVS Amino-acid change
ENST00000616242.5:c.-426T>G ENSP00000482149.2:n.-426T>G
ENST00000682635.1:n.61T>G
ENST00000403799.8:c.-426T>G MANE Select ENSP00000384247.3:n.-426T>G
ENST00000671824.1:c.-426T>G ENSP00000500264.1:n.-426T>G
ENST00000673284.1:c.-426T>G ENSP00000499852.1:n.-426T>G
ENST00000403799.7:c.-426T>G ENSP00000384247.3:n.-426T>G
ENST00000476008.1:n.480+8312T>G
NM_000162.3:c.-426T>G NP_000153.1:n.-426T>G
NM_000162.4:c.-426T>G NP_000153.1:n.-426T>G
NM_001354800.1:c.-426T>G NP_001341729.1:n.-426T>G
NM_000162.5:c.-426T>G MANE Select NP_000153.1:n.-426T>G
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