Canonical Allele Identifier: CA553568132

Gene: ADH7

Linked Data

• dbSNP Id: rs1399127932
• gnomAD v2: 4-100341670-TCTCAAA-T
• MyVariant Identifiers: chr4:g.100341671_100341676del (hg19) ; chr4:g.99420514_99420519del (hg38)

Genomic Alleles

HGVS	Genome Assembly
NC_000004.12:g.99420514_99420519del , CM000666.2:g.99420514_99420519del	GRCh38
NC_000004.11:g.100341671_100341676del , CM000666.1:g.100341671_100341676del	GRCh37
NC_000004.10:g.100560694_100560699del	NCBI36

Transcript Alleles

HGVS	Amino-acid Change
ENST00000437033.7:c.825+14_825+19del MANE Select	ENSP00000414254.2:n.825+14_825+19del
ENST00000209665.8:c.861+14_861+19del	ENSP00000209665.4:n.861+14_861+19del
ENST00000437033.6:c.825+14_825+19del	ENSP00000414254.2:n.825+14_825+19del
ENST00000476959.5:c.885+14_885+19del	ENSP00000420269.1:n.885+14_885+19del
ENST00000482593.5:c.654+14_654+19del	ENSP00000420613.1:n.654+14_654+19del
NM_000673.4:c.861+14_861+19del	NP_000664.2:n.861+14_861+19del
NM_001166504.1:c.885+14_885+19del	NP_001159976.1:n.885+14_885+19del
NM_000673.7:c.825+14_825+19del MANE Select	NP_000664.3:n.825+14_825+19del
NM_001166504.2:c.885+14_885+19del	NP_001159976.1:n.885+14_885+19del