Canonical Allele Identifier: CA1479994777
Gene: ADH7 HGNC NCBI

Linked Data

dbSNP Id: rs1721645597

Genomic Alleles

HGVS Genome Assembly
NC_000004.12:g.99421011_99421014del , CM000666.2:g.99421011_99421014del GRCh38
NC_000004.11:g.100342168_100342171del , CM000666.1:g.100342168_100342171del GRCh37
NC_000004.10:g.100561191_100561194del NCBI36

Transcript Alleles

HGVS Amino-acid Change
ENST00000437033.7:c.565-216_565-213del MANE Select ENSP00000414254.2:n.565-216_565-213del
ENST00000209665.8:c.601-216_601-213del ENSP00000209665.4:n.601-216_601-213del
ENST00000437033.6:c.565-216_565-213del ENSP00000414254.2:n.565-216_565-213del
ENST00000476959.5:c.625-216_625-213del ENSP00000420269.1:n.625-216_625-213del
ENST00000482593.5:c.394-216_394-213del ENSP00000420613.1:n.394-216_394-213del
NM_000673.4:c.601-216_601-213del NP_000664.2:n.601-216_601-213del
NM_001166504.1:c.625-216_625-213del NP_001159976.1:n.625-216_625-213del
NM_000673.7:c.565-216_565-213del MANE Select NP_000664.3:n.565-216_565-213del
NM_001166504.2:c.625-216_625-213del NP_001159976.1:n.625-216_625-213del