Canonical Allele Identifier: CA374562925

Gene: ALAD

Linked Data

• MyVariant Identifiers: chr9:g.116151269A>T (hg19) ; chr9:g.113388989A>T (hg38)

Genomic Alleles

HGVS	Genome Assembly
NC_000009.12:g.113388989A>T , CM000671.2:g.113388989A>T	GRCh38
NC_000009.11:g.116151269A>T , CM000671.1:g.116151269A>T	GRCh37
NC_000009.10:g.115191090A>T	NCBI36
NG_008716.1:g.17350T>A

Transcript Alleles

HGVS	Amino-acid Change
ENST00000409155.8:c.919T>A MANE Select	ENSP00000386284.3:p.Phe307Ile
ENST00000409155.7:c.919T>A	ENSP00000386284.3:p.Phe307Ile
ENST00000482847.5:n.1192T>A
NM_000031.5:c.919T>A	NP_000022.3:p.Phe307Ile
XM_005251799.1:c.1006T>A	XP_005251856.1:p.Phe336Ile
XM_011518363.1:c.1045T>A	XP_011516665.1:p.Phe349Ile
XM_011518364.1:c.946T>A	XP_011516666.1:p.Phe316Ile
NM_001003945.2:c.1006T>A	NP_001003945.1:p.Phe336Ile
NM_001317745.1:c.895T>A	NP_001304674.1:p.Phe299Ile
XM_011518364.2:c.946T>A	XP_011516666.1:p.Phe316Ile
XM_024447449.1:c.1006T>A	XP_024303217.1:p.Phe336Ile
NM_000031.6:c.919T>A MANE Select	NP_000022.3:p.Phe307Ile
NM_001003945.3:c.1006T>A	NP_001003945.1:p.Phe336Ile
NM_001317745.2:c.895T>A	NP_001304674.1:p.Phe299Ile