Canonical Allele Identifier: CA1479993568
Gene: ADH7 HGNC NCBI

Genomic Alleles

HGVS Genome Assembly
NC_000004.12:g.99420374_99420375delinsCA , CM000666.2:g.99420374_99420375delinsCA GRCh38
NC_000004.11:g.100341531_100341532delinsCA , CM000666.1:g.100341531_100341532delinsCA GRCh37
NC_000004.10:g.100560554_100560555delinsCA NCBI36

Transcript Alleles

HGVS Amino-acid Change
ENST00000437033.7:c.825+158_825+159delinsTG MANE Select ENSP00000414254.2:n.825+158_825+159delinsTG
ENST00000209665.8:c.861+158_861+159delinsTG ENSP00000209665.4:n.861+158_861+159delinsTG
ENST00000437033.6:c.825+158_825+159delinsTG ENSP00000414254.2:n.825+158_825+159delinsTG
ENST00000476959.5:c.885+158_885+159delinsTG ENSP00000420269.1:n.885+158_885+159delinsTG
ENST00000482593.5:c.654+158_654+159delinsTG ENSP00000420613.1:n.654+158_654+159delinsTG
NM_000673.4:c.861+158_861+159delinsTG NP_000664.2:n.861+158_861+159delinsTG
NM_001166504.1:c.885+158_885+159delinsTG NP_001159976.1:n.885+158_885+159delinsTG
NM_000673.7:c.825+158_825+159delinsTG MANE Select NP_000664.3:n.825+158_825+159delinsTG
NM_001166504.2:c.885+158_885+159delinsTG NP_001159976.1:n.885+158_885+159delinsTG