Canonical Allele Identifier: CA553108028

Gene: ADH7

Linked Data

• dbSNP Id: rs1256834279
• gnomAD v2: 4-100342100-AG-A
• MyVariant Identifiers: chr4:g.100342101del (hg19) ; chr4:g.99420944del (hg38)

Genomic Alleles

HGVS	Genome Assembly
NC_000004.12:g.99420946del , CM000666.2:g.99420946del	GRCh38
NC_000004.11:g.100342103del , CM000666.1:g.100342103del	GRCh37
NC_000004.10:g.100561126del	NCBI36

Transcript Alleles

HGVS	Amino-acid Change
ENST00000437033.7:c.565-151del MANE Select	ENSP00000414254.2:n.565-151del
ENST00000209665.8:c.601-151del	ENSP00000209665.4:n.601-151del
ENST00000437033.6:c.565-151del	ENSP00000414254.2:n.565-151del
ENST00000476959.5:c.625-151del	ENSP00000420269.1:n.625-151del
ENST00000482593.5:c.394-151del	ENSP00000420613.1:n.394-151del
NM_000673.4:c.601-151del	NP_000664.2:n.601-151del
NM_001166504.1:c.625-151del	NP_001159976.1:n.625-151del
NM_000673.7:c.565-151del MANE Select	NP_000664.3:n.565-151del
NM_001166504.2:c.625-151del	NP_001159976.1:n.625-151del