Canonical Allele Identifier: CA1479993507
Gene: ADH7 HGNC NCBI

Genomic Alleles

HGVS Genome Assembly
NC_000004.12:g.99420297_99420298delinsTA , CM000666.2:g.99420297_99420298delinsTA GRCh38
NC_000004.11:g.100341454_100341455delinsTA , CM000666.1:g.100341454_100341455delinsTA GRCh37
NC_000004.10:g.100560477_100560478delinsTA NCBI36

Transcript Alleles

HGVS Amino-acid Change
ENST00000437033.7:c.825+235_825+236delinsTA MANE Select ENSP00000414254.2:n.825+235_825+236delinsTA
ENST00000209665.8:c.861+235_861+236delinsTA ENSP00000209665.4:n.861+235_861+236delinsTA
ENST00000437033.6:c.825+235_825+236delinsTA ENSP00000414254.2:n.825+235_825+236delinsTA
ENST00000476959.5:c.885+235_885+236delinsTA ENSP00000420269.1:n.885+235_885+236delinsTA
ENST00000482593.5:c.654+235_654+236delinsTA ENSP00000420613.1:n.654+235_654+236delinsTA
NM_000673.4:c.861+235_861+236delinsTA NP_000664.2:n.861+235_861+236delinsTA
NM_001166504.1:c.885+235_885+236delinsTA NP_001159976.1:n.885+235_885+236delinsTA
NM_000673.7:c.825+235_825+236delinsTA MANE Select NP_000664.3:n.825+235_825+236delinsTA
NM_001166504.2:c.885+235_885+236delinsTA NP_001159976.1:n.885+235_885+236delinsTA