Canonical Allele Identifier: CA440318626

Gene: ADH7

Linked Data

• MyVariant Identifiers: chr4:g.100349674T>A (hg19)

Genomic Alleles

HGVS	Genome Assembly
NC_000004.12:g.99428517T>A , CM000666.2:g.99428517T>A	GRCh38
NC_000004.11:g.100349674T>A , CM000666.1:g.100349674T>A	GRCh37
NC_000004.10:g.100568697T>A	NCBI36

Transcript Alleles

HGVS	Amino-acid change
ENST00000437033.7:c.234A>T MANE Select	ENSP00000414254.2:p.Gly78=
ENST00000209665.8:c.270A>T	ENSP00000209665.4:p.Gly90=
ENST00000437033.6:c.234A>T	ENSP00000414254.2:p.Gly78=
ENST00000474027.1:c.63A>T	ENSP00000420300.1:p.Gly21=
ENST00000476959.5:c.294A>T	ENSP00000420269.1:p.Gly98=
ENST00000482593.5:c.63A>T	ENSP00000420613.1:p.Gly21=
NM_000673.4:c.270A>T	NP_000664.2:p.Gly90=
NM_001166504.1:c.294A>T	NP_001159976.1:p.Gly98=
NM_000673.7:c.234A>T MANE Select	NP_000664.3:p.Gly78=
NM_001166504.2:c.294A>T	NP_001159976.1:p.Gly98=