Canonical Allele Identifier: CA440506477

Gene: ADH7

Linked Data

• gnomAD v4: 4-99420737-G-T
• MyVariant Identifiers: chr4:g.100341894G>T (hg19)

Genomic Alleles

HGVS	Genome Assembly
NC_000004.12:g.99420737G>T , CM000666.2:g.99420737G>T	GRCh38
NC_000004.11:g.100341894G>T , CM000666.1:g.100341894G>T	GRCh37
NC_000004.10:g.100560917G>T	NCBI36

Transcript Alleles

HGVS	Amino-acid Change
ENST00000437033.7:c.621C>A MANE Select	ENSP00000414254.2:p.Val207=
ENST00000209665.8:c.657C>A	ENSP00000209665.4:p.Val219=
ENST00000437033.6:c.621C>A	ENSP00000414254.2:p.Val207=
ENST00000476959.5:c.681C>A	ENSP00000420269.1:p.Val227=
ENST00000482593.5:c.450C>A	ENSP00000420613.1:p.Val150=
NM_000673.4:c.657C>A	NP_000664.2:p.Val219=
NM_001166504.1:c.681C>A	NP_001159976.1:p.Val227=
NM_000673.7:c.621C>A MANE Select	NP_000664.3:p.Val207=
NM_001166504.2:c.681C>A	NP_001159976.1:p.Val227=