Canonical Allele Identifier: CA2682574980
Gene: GCK HGNC NCBI

Linked Data

gnomAD v4: 7-44189388-C-T
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Genomic Alleles

HGVS Genome Assembly
NC_000007.14:g.44189388C>T , CM000669.2:g.44189388C>T GRCh38
NC_000007.13:g.44228987C>T , CM000669.1:g.44228987C>T GRCh37
NC_000007.12:g.44195512C>T NCBI36
NG_008847.1:g.5036G>A
NG_008847.2:g.13783G>A

Transcript Alleles

HGVS Amino-acid change
ENST00000616242.5:c.-435G>A ENSP00000482149.2:n.-435G>A
ENST00000682635.1:n.52G>A
ENST00000403799.8:c.-435G>A MANE Select ENSP00000384247.3:n.-435G>A
ENST00000671824.1:c.-435G>A ENSP00000500264.1:n.-435G>A
ENST00000673284.1:c.-435G>A ENSP00000499852.1:n.-435G>A
ENST00000403799.7:c.-435G>A ENSP00000384247.3:n.-435G>A
ENST00000476008.1:n.480+8303G>A
NM_000162.3:c.-435G>A NP_000153.1:n.-435G>A
NM_000162.4:c.-435G>A NP_000153.1:n.-435G>A
NM_001354800.1:c.-435G>A NP_001341729.1:n.-435G>A
NM_000162.5:c.-435G>A MANE Select NP_000153.1:n.-435G>A
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