Canonical Allele Identifier: CA1479993657
Gene: ADH7 HGNC NCBI

Linked Data

dbSNP Id: rs1721620190

Genomic Alleles

HGVS Genome Assembly
NC_000004.12:g.99420449del , CM000666.2:g.99420449del GRCh38
NC_000004.11:g.100341606del , CM000666.1:g.100341606del GRCh37
NC_000004.10:g.100560629del NCBI36

Transcript Alleles

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