Canonical Allele Identifier: CA5196329

Gene: ALAD

Linked Data

• ClinVar Variation Id: 913818
• ClinVar RCV Id: RCV001167638
• dbSNP Id: rs759917153
• ExAC: 9:116151318 C / T
• gnomAD v2: 9-116151318-C-T
• gnomAD v3: 9-113389038-C-T
• gnomAD v4: 9-113389038-C-T
• MyVariant Identifiers: chr9:g.116151318C>T (hg19) ; chr9:g.113389038C>T (hg38)

Genomic Alleles

HGVS	Genome Assembly
NC_000009.12:g.113389038C>T , CM000671.2:g.113389038C>T	GRCh38
NC_000009.11:g.116151318C>T , CM000671.1:g.116151318C>T	GRCh37
NC_000009.10:g.115191139C>T	NCBI36
NG_008716.1:g.17301G>A

Transcript Alleles

HGVS	Amino-acid Change
ENST00000409155.8:c.870G>A MANE Select	ENSP00000386284.3:p.Gln290=
ENST00000409155.7:c.870G>A	ENSP00000386284.3:p.Gln290=
ENST00000482847.5:n.1143G>A
NM_000031.5:c.870G>A	NP_000022.3:p.Gln290=
XM_005251799.1:c.957G>A	XP_005251856.1:p.Gln319=
XM_011518363.1:c.996G>A	XP_011516665.1:p.Gln332=
XM_011518364.1:c.897G>A	XP_011516666.1:p.Gln299=
NM_001003945.2:c.957G>A	NP_001003945.1:p.Gln319=
NM_001317745.1:c.846G>A	NP_001304674.1:p.Gln282=
XM_011518364.2:c.897G>A	XP_011516666.1:p.Gln299=
XM_024447449.1:c.957G>A	XP_024303217.1:p.Gln319=
NM_000031.6:c.870G>A MANE Select	NP_000022.3:p.Gln290=
NM_001003945.3:c.957G>A	NP_001003945.1:p.Gln319=
NM_001317745.2:c.846G>A	NP_001304674.1:p.Gln282=