Canonical Allele Identifier: CA1479993653
Gene: ADH7 HGNC NCBI

Genomic Alleles

HGVS Genome Assembly
NC_000004.12:g.99420445_99420446delinsCT , CM000666.2:g.99420445_99420446delinsCT GRCh38
NC_000004.11:g.100341602_100341603delinsCT , CM000666.1:g.100341602_100341603delinsCT GRCh37
NC_000004.10:g.100560625_100560626delinsCT NCBI36

Transcript Alleles

HGVS Amino-acid Change
ENST00000437033.7:c.825+87_825+88delinsAG MANE Select ENSP00000414254.2:n.825+87_825+88delinsAG
ENST00000209665.8:c.861+87_861+88delinsAG ENSP00000209665.4:n.861+87_861+88delinsAG
ENST00000437033.6:c.825+87_825+88delinsAG ENSP00000414254.2:n.825+87_825+88delinsAG
ENST00000476959.5:c.885+87_885+88delinsAG ENSP00000420269.1:n.885+87_885+88delinsAG
ENST00000482593.5:c.654+87_654+88delinsAG ENSP00000420613.1:n.654+87_654+88delinsAG
NM_000673.4:c.861+87_861+88delinsAG NP_000664.2:n.861+87_861+88delinsAG
NM_001166504.1:c.885+87_885+88delinsAG NP_001159976.1:n.885+87_885+88delinsAG
NM_000673.7:c.825+87_825+88delinsAG MANE Select NP_000664.3:n.825+87_825+88delinsAG
NM_001166504.2:c.885+87_885+88delinsAG NP_001159976.1:n.885+87_885+88delinsAG