Canonical Allele Identifier: CA2682574989
Gene: GCK HGNC NCBI

Linked Data

gnomAD v4: 7-44189391-T-G
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Genomic Alleles

HGVS Genome Assembly
NC_000007.14:g.44189391T>G , CM000669.2:g.44189391T>G GRCh38
NC_000007.13:g.44228990T>G , CM000669.1:g.44228990T>G GRCh37
NC_000007.12:g.44195515T>G NCBI36
NG_008847.1:g.5033A>C
NG_008847.2:g.13780A>C

Transcript Alleles

HGVS Amino-acid change
ENST00000616242.5:c.-438A>C ENSP00000482149.2:n.-438A>C
ENST00000682635.1:n.49A>C
ENST00000403799.8:c.-438A>C MANE Select ENSP00000384247.3:n.-438A>C
ENST00000671824.1:c.-438A>C ENSP00000500264.1:n.-438A>C
ENST00000673284.1:c.-438A>C ENSP00000499852.1:n.-438A>C
ENST00000403799.7:c.-438A>C ENSP00000384247.3:n.-438A>C
ENST00000476008.1:n.480+8300A>C
NM_000162.3:c.-438A>C NP_000153.1:n.-438A>C
NM_000162.4:c.-438A>C NP_000153.1:n.-438A>C
NM_001354800.1:c.-438A>C NP_001341729.1:n.-438A>C
NM_000162.5:c.-438A>C MANE Select NP_000153.1:n.-438A>C
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