Canonical Allele Identifier: CA3020722

Gene: ADH7

Linked Data

• dbSNP Id: rs770480873
• ExAC: 4:100341685 C / T
• MyVariant Identifiers: chr4:g.100341685C>T (hg19) ; chr4:g.99420528C>T (hg38)

Genomic Alleles

HGVS	Genome Assembly
NC_000004.12:g.99420528C>T , CM000666.2:g.99420528C>T	GRCh38
NC_000004.11:g.100341685C>T , CM000666.1:g.100341685C>T	GRCh37
NC_000004.10:g.100560708C>T	NCBI36

Transcript Alleles

HGVS	Amino-acid Change
ENST00000437033.7:c.825+5G>A MANE Select	ENSP00000414254.2:n.825+5G>A
ENST00000209665.8:c.861+5G>A	ENSP00000209665.4:n.861+5G>A
ENST00000437033.6:c.825+5G>A	ENSP00000414254.2:n.825+5G>A
ENST00000476959.5:c.885+5G>A	ENSP00000420269.1:n.885+5G>A
ENST00000482593.5:c.654+5G>A	ENSP00000420613.1:n.654+5G>A
NM_000673.4:c.861+5G>A	NP_000664.2:n.861+5G>A
NM_001166504.1:c.885+5G>A	NP_001159976.1:n.885+5G>A
NM_000673.7:c.825+5G>A MANE Select	NP_000664.3:n.825+5G>A
NM_001166504.2:c.885+5G>A	NP_001159976.1:n.885+5G>A