Canonical Allele Identifier: CA1479993629

Gene: ADH7

Genomic Alleles

HGVS	Genome Assembly
NC_000004.12:g.99420412_99420416delinsAACTG , CM000666.2:g.99420412_99420416delinsAACTG	GRCh38
NC_000004.11:g.100341569_100341573delinsAACTG , CM000666.1:g.100341569_100341573delinsAACTG	GRCh37
NC_000004.10:g.100560592_100560596delinsAACTG	NCBI36

Transcript Alleles

HGVS	Amino-acid Change
ENST00000437033.7:c.825+117_825+121delinsCAGTT MANE Select	ENSP00000414254.2:n.825+117_825+121delinsCAGTT
ENST00000209665.8:c.861+117_861+121delinsCAGTT	ENSP00000209665.4:n.861+117_861+121delinsCAGTT
ENST00000437033.6:c.825+117_825+121delinsCAGTT	ENSP00000414254.2:n.825+117_825+121delinsCAGTT
ENST00000476959.5:c.885+117_885+121delinsCAGTT	ENSP00000420269.1:n.885+117_885+121delinsCAGTT
ENST00000482593.5:c.654+117_654+121delinsCAGTT	ENSP00000420613.1:n.654+117_654+121delinsCAGTT
NM_000673.4:c.861+117_861+121delinsCAGTT	NP_000664.2:n.861+117_861+121delinsCAGTT
NM_001166504.1:c.885+117_885+121delinsCAGTT	NP_001159976.1:n.885+117_885+121delinsCAGTT
NM_000673.7:c.825+117_825+121delinsCAGTT MANE Select	NP_000664.3:n.825+117_825+121delinsCAGTT
NM_001166504.2:c.885+117_885+121delinsCAGTT	NP_001159976.1:n.885+117_885+121delinsCAGTT