Canonical Allele Identifier: CA800742562

Gene: ADH7

Linked Data

• dbSNP Id: rs1462774998
• MyVariant Identifiers: chr4:g.100342154_100342157del (hg19) ; chr4:g.99420997_99421000del (hg38)

Genomic Alleles

HGVS	Genome Assembly
NC_000004.12:g.99420999_99421002del , CM000666.2:g.99420999_99421002del	GRCh38
NC_000004.11:g.100342156_100342159del , CM000666.1:g.100342156_100342159del	GRCh37
NC_000004.10:g.100561179_100561182del	NCBI36

Transcript Alleles

HGVS	Amino-acid Change
ENST00000437033.7:c.565-207_565-204del MANE Select	ENSP00000414254.2:n.565-207_565-204del
ENST00000209665.8:c.601-207_601-204del	ENSP00000209665.4:n.601-207_601-204del
ENST00000437033.6:c.565-207_565-204del	ENSP00000414254.2:n.565-207_565-204del
ENST00000476959.5:c.625-207_625-204del	ENSP00000420269.1:n.625-207_625-204del
ENST00000482593.5:c.394-207_394-204del	ENSP00000420613.1:n.394-207_394-204del
NM_000673.4:c.601-207_601-204del	NP_000664.2:n.601-207_601-204del
NM_001166504.1:c.625-207_625-204del	NP_001159976.1:n.625-207_625-204del
NM_000673.7:c.565-207_565-204del MANE Select	NP_000664.3:n.565-207_565-204del
NM_001166504.2:c.625-207_625-204del	NP_001159976.1:n.625-207_625-204del