Canonical Allele Identifier: CA2671525019
Gene: ADH7 HGNC NCBI

Linked Data

gnomAD v4: 4-99420398-T-A

Genomic Alleles

HGVS Genome Assembly
NC_000004.12:g.99420398T>A , CM000666.2:g.99420398T>A GRCh38
NC_000004.11:g.100341555T>A , CM000666.1:g.100341555T>A GRCh37
NC_000004.10:g.100560578T>A NCBI36

Transcript Alleles

HGVS Amino-acid Change
ENST00000437033.7:c.825+135A>T MANE Select ENSP00000414254.2:n.825+135A>T
ENST00000209665.8:c.861+135A>T ENSP00000209665.4:n.861+135A>T
ENST00000437033.6:c.825+135A>T ENSP00000414254.2:n.825+135A>T
ENST00000476959.5:c.885+135A>T ENSP00000420269.1:n.885+135A>T
ENST00000482593.5:c.654+135A>T ENSP00000420613.1:n.654+135A>T
NM_000673.4:c.861+135A>T NP_000664.2:n.861+135A>T
NM_001166504.1:c.885+135A>T NP_001159976.1:n.885+135A>T
NM_000673.7:c.825+135A>T MANE Select NP_000664.3:n.825+135A>T
NM_001166504.2:c.885+135A>T NP_001159976.1:n.885+135A>T