Canonical Allele Identifier: CA1480005358
Gene: ADH7 HGNC NCBI

Genomic Alleles

HGVS Genome Assembly
NC_000004.12:g.99428579T= , CM000666.2:g.99428579T= GRCh38
NC_000004.11:g.100349736T= , CM000666.1:g.100349736T= GRCh37
NC_000004.10:g.100568759T= NCBI36

Transcript Alleles

HGVS Amino-acid Change
ENST00000437033.7:c.172A= MANE Select ENSP00000414254.2:p.Met58=
ENST00000209665.8:c.208A= ENSP00000209665.4:p.Met70=
ENST00000437033.6:c.172A= ENSP00000414254.2:p.Met58=
ENST00000474027.1:c.1A= ENSP00000420300.1:p.Met1=
ENST00000476959.5:c.232A= ENSP00000420269.1:p.Met78=
ENST00000482593.5:c.1A= ENSP00000420613.1:p.Met1=
NM_000673.4:c.208A= NP_000664.2:p.Met70=
NM_001166504.1:c.232A= NP_001159976.1:p.Met78=
NM_000673.7:c.172A= MANE Select NP_000664.3:p.Met58=
NM_001166504.2:c.232A= NP_001159976.1:p.Met78=