Canonical Allele Identifier: CA2671525029
Gene: ADH7 HGNC NCBI

Linked Data

gnomAD v4: 4-99420414-C-A

Genomic Alleles

HGVS Genome Assembly
NC_000004.12:g.99420414C>A , CM000666.2:g.99420414C>A GRCh38
NC_000004.11:g.100341571C>A , CM000666.1:g.100341571C>A GRCh37
NC_000004.10:g.100560594C>A NCBI36

Transcript Alleles

HGVS Amino-acid Change
ENST00000437033.7:c.825+119G>T MANE Select ENSP00000414254.2:n.825+119G>T
ENST00000209665.8:c.861+119G>T ENSP00000209665.4:n.861+119G>T
ENST00000437033.6:c.825+119G>T ENSP00000414254.2:n.825+119G>T
ENST00000476959.5:c.885+119G>T ENSP00000420269.1:n.885+119G>T
ENST00000482593.5:c.654+119G>T ENSP00000420613.1:n.654+119G>T
NM_000673.4:c.861+119G>T NP_000664.2:n.861+119G>T
NM_001166504.1:c.885+119G>T NP_001159976.1:n.885+119G>T
NM_000673.7:c.825+119G>T MANE Select NP_000664.3:n.825+119G>T
NM_001166504.2:c.885+119G>T NP_001159976.1:n.885+119G>T