Canonical Allele Identifier: CA466758208

Gene: ALAD

Linked Data

• MyVariant Identifiers: chr9:g.116153825G>T (hg19)

Genomic Alleles

HGVS	Genome Assembly
NC_000009.12:g.113391545G>T , CM000671.2:g.113391545G>T	GRCh38
NC_000009.11:g.116153825G>T , CM000671.1:g.116153825G>T	GRCh37
NC_000009.10:g.115193646G>T	NCBI36
NG_008716.1:g.14794C>A

Transcript Alleles

HGVS	Amino-acid change
ENST00000409155.8:c.243C>A MANE Select	ENSP00000386284.3:p.Val81=
ENST00000409155.7:c.243C>A	ENSP00000386284.3:p.Val81=
ENST00000448137.5:c.270C>A	ENSP00000392748.1:p.Val90=
ENST00000464749.5:n.258-612C>A
ENST00000468504.5:n.365C>A
ENST00000482001.1:n.516C>A
ENST00000482847.5:n.516C>A
NM_000031.5:c.243C>A	NP_000022.3:p.Val81=
XM_005251799.1:c.330C>A	XP_005251856.1:p.Val110=
XM_011518363.1:c.369C>A	XP_011516665.1:p.Val123=
XM_011518364.1:c.270C>A	XP_011516666.1:p.Val90=
NM_001003945.2:c.330C>A	NP_001003945.1:p.Val110=
NM_001317745.1:c.219C>A	NP_001304674.1:p.Val73=
XM_011518364.2:c.270C>A	XP_011516666.1:p.Val90=
XM_024447449.1:c.330C>A	XP_024303217.1:p.Val110=
XR_002956764.1:n.743C>A
NM_000031.6:c.243C>A MANE Select	NP_000022.3:p.Val81=
NM_001003945.3:c.330C>A	NP_001003945.1:p.Val110=
NM_001317745.2:c.219C>A	NP_001304674.1:p.Val73=