Canonical Allele Identifier: CA440506439

Gene: ADH7

Linked Data

• gnomAD v4: 4-99420683-G-A
• MyVariant Identifiers: chr4:g.100341840G>A (hg19)

Genomic Alleles

HGVS	Genome Assembly
NC_000004.12:g.99420683G>A , CM000666.2:g.99420683G>A	GRCh38
NC_000004.11:g.100341840G>A , CM000666.1:g.100341840G>A	GRCh37
NC_000004.10:g.100560863G>A	NCBI36

Transcript Alleles

HGVS	Amino-acid Change
ENST00000437033.7:c.675C>T MANE Select	ENSP00000414254.2:p.Asn225=
ENST00000209665.8:c.711C>T	ENSP00000209665.4:p.Asn237=
ENST00000437033.6:c.675C>T	ENSP00000414254.2:p.Asn225=
ENST00000476959.5:c.735C>T	ENSP00000420269.1:p.Asn245=
ENST00000482593.5:c.504C>T	ENSP00000420613.1:p.Asn168=
NM_000673.4:c.711C>T	NP_000664.2:p.Asn237=
NM_001166504.1:c.735C>T	NP_001159976.1:p.Asn245=
NM_000673.7:c.675C>T MANE Select	NP_000664.3:p.Asn225=
NM_001166504.2:c.735C>T	NP_001159976.1:p.Asn245=