Canonical Allele Identifier: CA858872429

Gene: ALAD

Linked Data

• dbSNP Id: rs1168144285
• gnomAD v3: 9-113391751-A-G
• gnomAD v4: 9-113391751-A-G
• MyVariant Identifiers: chr9:g.116154031A>G (hg19) ; chr9:g.113391751A>G (hg38)

Genomic Alleles

HGVS	Genome Assembly
NC_000009.12:g.113391751A>G , CM000671.2:g.113391751A>G	GRCh38
NC_000009.11:g.116154031A>G , CM000671.1:g.116154031A>G	GRCh37
NC_000009.10:g.115193852A>G	NCBI36
NG_008716.1:g.14588T>C

Transcript Alleles

HGVS	Amino-acid Change
ENST00000409155.8:c.165-128T>C MANE Select	ENSP00000386284.3:n.165-128T>C
ENST00000409155.7:c.165-128T>C	ENSP00000386284.3:n.165-128T>C
ENST00000448137.5:c.192-128T>C	ENSP00000392748.1:n.192-128T>C
ENST00000464749.5:n.258-818T>C
ENST00000468504.5:n.287-128T>C
ENST00000482001.1:n.438-128T>C
ENST00000482847.5:n.438-128T>C
NM_000031.5:c.165-128T>C	NP_000022.3:n.165-128T>C
XM_005251799.1:c.252-128T>C	XP_005251856.1:n.252-128T>C
XM_011518363.1:c.291-128T>C	XP_011516665.1:n.291-128T>C
XM_011518364.1:c.192-128T>C	XP_011516666.1:n.192-128T>C
NM_001003945.2:c.252-128T>C	NP_001003945.1:n.252-128T>C
NM_001317745.1:c.141-128T>C	NP_001304674.1:n.141-128T>C
XM_011518364.2:c.192-128T>C	XP_011516666.1:n.192-128T>C
XM_024447449.1:c.252-128T>C	XP_024303217.1:n.252-128T>C
XR_002956764.1:n.665-128T>C
NM_000031.6:c.165-128T>C MANE Select	NP_000022.3:n.165-128T>C
NM_001003945.3:c.252-128T>C	NP_001003945.1:n.252-128T>C
NM_001317745.2:c.141-128T>C	NP_001304674.1:n.141-128T>C