Canonical Allele Identifier: CA553108021

Gene: ADH7

Linked Data

• gnomAD v2: 4-100342023-T-A
• gnomAD v4: 4-99420866-T-A
• MyVariant Identifiers: chr4:g.100342023T>A (hg19) ; chr4:g.99420866T>A (hg38)

Genomic Alleles

HGVS	Genome Assembly
NC_000004.12:g.99420866T>A , CM000666.2:g.99420866T>A	GRCh38
NC_000004.11:g.100342023T>A , CM000666.1:g.100342023T>A	GRCh37
NC_000004.10:g.100561046T>A	NCBI36

Transcript Alleles

HGVS	Amino-acid Change
ENST00000437033.7:c.565-73A>T MANE Select	ENSP00000414254.2:n.565-73A>T
ENST00000209665.8:c.601-73A>T	ENSP00000209665.4:n.601-73A>T
ENST00000437033.6:c.565-73A>T	ENSP00000414254.2:n.565-73A>T
ENST00000476959.5:c.625-73A>T	ENSP00000420269.1:n.625-73A>T
ENST00000482593.5:c.394-73A>T	ENSP00000420613.1:n.394-73A>T
NM_000673.4:c.601-73A>T	NP_000664.2:n.601-73A>T
NM_001166504.1:c.625-73A>T	NP_001159976.1:n.625-73A>T
NM_000673.7:c.565-73A>T MANE Select	NP_000664.3:n.565-73A>T
NM_001166504.2:c.625-73A>T	NP_001159976.1:n.625-73A>T