Canonical Allele Identifier: CA374565051

Gene: ALAD

Linked Data

• MyVariant Identifiers: chr9:g.116153841A>T (hg19) ; chr9:g.113391561A>T (hg38)

Genomic Alleles

HGVS	Genome Assembly
NC_000009.12:g.113391561A>T , CM000671.2:g.113391561A>T	GRCh38
NC_000009.11:g.116153841A>T , CM000671.1:g.116153841A>T	GRCh37
NC_000009.10:g.115193662A>T	NCBI36
NG_008716.1:g.14778T>A

Transcript Alleles

HGVS	Amino-acid Change
ENST00000409155.8:c.227T>A MANE Select	ENSP00000386284.3:p.Val76Asp
ENST00000409155.7:c.227T>A	ENSP00000386284.3:p.Val76Asp
ENST00000448137.5:c.254T>A	ENSP00000392748.1:p.Val85Asp
ENST00000464749.5:n.258-628T>A
ENST00000468504.5:n.349T>A
ENST00000482001.1:n.500T>A
ENST00000482847.5:n.500T>A
NM_000031.5:c.227T>A	NP_000022.3:p.Val76Asp
XM_005251799.1:c.314T>A	XP_005251856.1:p.Val105Asp
XM_011518363.1:c.353T>A	XP_011516665.1:p.Val118Asp
XM_011518364.1:c.254T>A	XP_011516666.1:p.Val85Asp
NM_001003945.2:c.314T>A	NP_001003945.1:p.Val105Asp
NM_001317745.1:c.203T>A	NP_001304674.1:p.Val68Asp
XM_011518364.2:c.254T>A	XP_011516666.1:p.Val85Asp
XM_024447449.1:c.314T>A	XP_024303217.1:p.Val105Asp
XR_002956764.1:n.727T>A
NM_000031.6:c.227T>A MANE Select	NP_000022.3:p.Val76Asp
NM_001003945.3:c.314T>A	NP_001003945.1:p.Val105Asp
NM_001317745.2:c.203T>A	NP_001304674.1:p.Val68Asp