Canonical Allele Identifier: CA1479993656
Gene: ADH7 HGNC NCBI

Genomic Alleles

HGVS Genome Assembly
NC_000004.12:g.99420447_99420448delinsAT , CM000666.2:g.99420447_99420448delinsAT GRCh38
NC_000004.11:g.100341604_100341605delinsAT , CM000666.1:g.100341604_100341605delinsAT GRCh37
NC_000004.10:g.100560627_100560628delinsAT NCBI36

Transcript Alleles

HGVS Amino-acid Change
ENST00000437033.7:c.825+85_825+86delinsAT MANE Select ENSP00000414254.2:n.825+85_825+86delinsAT
ENST00000209665.8:c.861+85_861+86delinsAT ENSP00000209665.4:n.861+85_861+86delinsAT
ENST00000437033.6:c.825+85_825+86delinsAT ENSP00000414254.2:n.825+85_825+86delinsAT
ENST00000476959.5:c.885+85_885+86delinsAT ENSP00000420269.1:n.885+85_885+86delinsAT
ENST00000482593.5:c.654+85_654+86delinsAT ENSP00000420613.1:n.654+85_654+86delinsAT
NM_000673.4:c.861+85_861+86delinsAT NP_000664.2:n.861+85_861+86delinsAT
NM_001166504.1:c.885+85_885+86delinsAT NP_001159976.1:n.885+85_885+86delinsAT
NM_000673.7:c.825+85_825+86delinsAT MANE Select NP_000664.3:n.825+85_825+86delinsAT
NM_001166504.2:c.885+85_885+86delinsAT NP_001159976.1:n.885+85_885+86delinsAT