Canonical Allele Identifier: CA5196670

Gene: ALAD

Linked Data

• ClinVar Variation Id: 2041998
• ClinVar RCV Id: RCV002903407
• dbSNP Id: rs121912984
• ExAC: 9:116155804 G / A
• gnomAD v2: 9-116155804-G-A
• gnomAD v4: 9-113393524-G-A
• MyVariant Identifiers: chr9:g.116155804G>A (hg19) ; chr9:g.113393524G>A (hg38)

Genomic Alleles

HGVS	Genome Assembly
NC_000009.12:g.113393524G>A , CM000671.2:g.113393524G>A	GRCh38
NC_000009.11:g.116155804G>A , CM000671.1:g.116155804G>A	GRCh37
NC_000009.10:g.115195625G>A	NCBI36
NG_008716.1:g.12815C>T

Transcript Alleles

HGVS	Amino-acid change
ENST00000409155.8:c.36C>T MANE Select	ENSP00000386284.3:p.Phe12=
ENST00000409155.7:c.36C>T	ENSP00000386284.3:p.Phe12=
ENST00000448137.5:c.63C>T	ENSP00000392748.1:p.Phe21=
ENST00000452726.1:c.63C>T	ENSP00000415737.1:p.Phe21=
ENST00000464749.5:n.180C>T
ENST00000468504.5:n.158C>T
ENST00000482847.5:n.143C>T
ENST00000494848.1:n.184C>T
NM_000031.5:c.36C>T	NP_000022.3:p.Phe12=
XM_005251799.1:c.-44C>T	XP_005251856.1:n.-44C>T
XM_011518363.1:c.162C>T	XP_011516665.1:p.Phe54=
XM_011518364.1:c.63C>T	XP_011516666.1:p.Phe21=
NM_001003945.2:c.-44C>T	NP_001003945.1:n.-44C>T
NM_001317745.1:c.63C>T	NP_001304674.1:p.Phe21=
XM_011518364.2:c.63C>T	XP_011516666.1:p.Phe21=
XM_024447449.1:c.-44C>T	XP_024303217.1:n.-44C>T
XR_002956764.1:n.536C>T
NM_000031.6:c.36C>T MANE Select	NP_000022.3:p.Phe12=
NM_001003945.3:c.-44C>T	NP_001003945.1:n.-44C>T
NM_001317745.2:c.63C>T	NP_001304674.1:p.Phe21=