Canonical Allele Identifier: CA1479993614

Gene: ADH7

Linked Data

• dbSNP Id: rs1721619130
• gnomAD v4: 4-99420396-G-GTT

Genomic Alleles

HGVS	Genome Assembly
NC_000004.12:g.99420400_99420401dup , CM000666.2:g.99420400_99420401dup	GRCh38
NC_000004.11:g.100341557_100341558dup , CM000666.1:g.100341557_100341558dup	GRCh37
NC_000004.10:g.100560580_100560581dup	NCBI36

Transcript Alleles

HGVS	Amino-acid Change
ENST00000437033.7:c.825+135_825+136dup MANE Select	ENSP00000414254.2:n.825+135_825+136dup
ENST00000209665.8:c.861+135_861+136dup	ENSP00000209665.4:n.861+135_861+136dup
ENST00000437033.6:c.825+135_825+136dup	ENSP00000414254.2:n.825+135_825+136dup
ENST00000476959.5:c.885+135_885+136dup	ENSP00000420269.1:n.885+135_885+136dup
ENST00000482593.5:c.654+135_654+136dup	ENSP00000420613.1:n.654+135_654+136dup
NM_000673.4:c.861+135_861+136dup	NP_000664.2:n.861+135_861+136dup
NM_001166504.1:c.885+135_885+136dup	NP_001159976.1:n.885+135_885+136dup
NM_000673.7:c.825+135_825+136dup MANE Select	NP_000664.3:n.825+135_825+136dup
NM_001166504.2:c.885+135_885+136dup	NP_001159976.1:n.885+135_885+136dup