Canonical Allele Identifier: CA1479993808
Gene: ADH7 HGNC NCBI

Genomic Alleles

HGVS Genome Assembly
NC_000004.12:g.99420556C= , CM000666.2:g.99420556C= GRCh38
NC_000004.11:g.100341713C= , CM000666.1:g.100341713C= GRCh37
NC_000004.10:g.100560736C= NCBI36

Transcript Alleles

HGVS Amino-acid Change
ENST00000437033.7:c.802G= MANE Select ENSP00000414254.2:p.Val268=
ENST00000209665.8:c.838G= ENSP00000209665.4:p.Val280=
ENST00000437033.6:c.802G= ENSP00000414254.2:p.Val268=
ENST00000476959.5:c.862G= ENSP00000420269.1:p.Val288=
ENST00000482593.5:c.631G= ENSP00000420613.1:p.Val211=
NM_000673.4:c.838G= NP_000664.2:p.Val280=
NM_001166504.1:c.862G= NP_001159976.1:p.Val288=
NM_000673.7:c.802G= MANE Select NP_000664.3:p.Val268=
NM_001166504.2:c.862G= NP_001159976.1:p.Val288=