Canonical Allele Identifier: CA2671525471

Gene: ADH7

Linked Data

• gnomAD v4: 4-99428442-C-CTAA

Genomic Alleles

HGVS	Genome Assembly
NC_000004.12:g.99428444_99428446dup , CM000666.2:g.99428444_99428446dup	GRCh38
NC_000004.11:g.100349601_100349603dup , CM000666.1:g.100349601_100349603dup	GRCh37
NC_000004.10:g.100568624_100568626dup	NCBI36

Transcript Alleles

HGVS	Amino-acid change
ENST00000437033.7:c.259+47_259+49dup MANE Select	ENSP00000414254.2:n.259+47_259+49dup
ENST00000209665.8:c.295+47_295+49dup	ENSP00000209665.4:n.295+47_295+49dup
ENST00000437033.6:c.259+47_259+49dup	ENSP00000414254.2:n.259+47_259+49dup
ENST00000474027.1:c.88+47_88+49dup	ENSP00000420300.1:n.88+47_88+49dup
ENST00000476959.5:c.319+47_319+49dup	ENSP00000420269.1:n.319+47_319+49dup
ENST00000482593.5:c.88+47_88+49dup	ENSP00000420613.1:n.88+47_88+49dup
NM_000673.4:c.295+47_295+49dup	NP_000664.2:n.295+47_295+49dup
NM_001166504.1:c.319+47_319+49dup	NP_001159976.1:n.319+47_319+49dup
NM_000673.7:c.259+47_259+49dup MANE Select	NP_000664.3:n.259+47_259+49dup
NM_001166504.2:c.319+47_319+49dup	NP_001159976.1:n.319+47_319+49dup