Canonical Allele Identifier: CA5196328

Gene: ALAD

Linked Data

• ClinVar Variation Id: 1576829
• ClinVar RCV Id: RCV002085573
• dbSNP Id: rs200378521
• ExAC: 9:116151315 G / A
• gnomAD v2: 9-116151315-G-A
• gnomAD v3: 9-113389035-G-A
• gnomAD v4: 9-113389035-G-A
• MyVariant Identifiers: chr9:g.116151315G>A (hg19) ; chr9:g.113389035G>A (hg38)

Genomic Alleles

HGVS	Genome Assembly
NC_000009.12:g.113389035G>A , CM000671.2:g.113389035G>A	GRCh38
NC_000009.11:g.116151315G>A , CM000671.1:g.116151315G>A	GRCh37
NC_000009.10:g.115191136G>A	NCBI36
NG_008716.1:g.17304C>T

Transcript Alleles

HGVS	Amino-acid Change
ENST00000409155.8:c.873C>T MANE Select	ENSP00000386284.3:p.Ala291=
ENST00000409155.7:c.873C>T	ENSP00000386284.3:p.Ala291=
ENST00000482847.5:n.1146C>T
NM_000031.5:c.873C>T	NP_000022.3:p.Ala291=
XM_005251799.1:c.960C>T	XP_005251856.1:p.Ala320=
XM_011518363.1:c.999C>T	XP_011516665.1:p.Ala333=
XM_011518364.1:c.900C>T	XP_011516666.1:p.Ala300=
NM_001003945.2:c.960C>T	NP_001003945.1:p.Ala320=
NM_001317745.1:c.849C>T	NP_001304674.1:p.Ala283=
XM_011518364.2:c.900C>T	XP_011516666.1:p.Ala300=
XM_024447449.1:c.960C>T	XP_024303217.1:p.Ala320=
NM_000031.6:c.873C>T MANE Select	NP_000022.3:p.Ala291=
NM_001003945.3:c.960C>T	NP_001003945.1:p.Ala320=
NM_001317745.2:c.849C>T	NP_001304674.1:p.Ala283=