Canonical Allele Identifier: CA466755088

Gene: ALAD

Linked Data

• MyVariant Identifiers: chr9:g.116151309T>A (hg19)

Genomic Alleles

HGVS	Genome Assembly
NC_000009.12:g.113389029T>A , CM000671.2:g.113389029T>A	GRCh38
NC_000009.11:g.116151309T>A , CM000671.1:g.116151309T>A	GRCh37
NC_000009.10:g.115191130T>A	NCBI36
NG_008716.1:g.17310A>T

Transcript Alleles

HGVS	Amino-acid Change
ENST00000409155.8:c.879A>T MANE Select	ENSP00000386284.3:p.Ala293=
ENST00000409155.7:c.879A>T	ENSP00000386284.3:p.Ala293=
ENST00000482847.5:n.1152A>T
NM_000031.5:c.879A>T	NP_000022.3:p.Ala293=
XM_005251799.1:c.966A>T	XP_005251856.1:p.Ala322=
XM_011518363.1:c.1005A>T	XP_011516665.1:p.Ala335=
XM_011518364.1:c.906A>T	XP_011516666.1:p.Ala302=
NM_001003945.2:c.966A>T	NP_001003945.1:p.Ala322=
NM_001317745.1:c.855A>T	NP_001304674.1:p.Ala285=
XM_011518364.2:c.906A>T	XP_011516666.1:p.Ala302=
XM_024447449.1:c.966A>T	XP_024303217.1:p.Ala322=
NM_000031.6:c.879A>T MANE Select	NP_000022.3:p.Ala293=
NM_001003945.3:c.966A>T	NP_001003945.1:p.Ala322=
NM_001317745.2:c.855A>T	NP_001304674.1:p.Ala285=