Canonical Allele Identifier: CA466758260

Gene: ALAD

Linked Data

• MyVariant Identifiers: chr9:g.116153888C>G (hg19)

Genomic Alleles

HGVS	Genome Assembly
NC_000009.12:g.113391608C>G , CM000671.2:g.113391608C>G	GRCh38
NC_000009.11:g.116153888C>G , CM000671.1:g.116153888C>G	GRCh37
NC_000009.10:g.115193709C>G	NCBI36
NG_008716.1:g.14731G>C

Transcript Alleles

HGVS	Amino-acid Change
ENST00000409155.8:c.180G>C MANE Select	ENSP00000386284.3:p.Arg60=
ENST00000409155.7:c.180G>C	ENSP00000386284.3:p.Arg60=
ENST00000448137.5:c.207G>C	ENSP00000392748.1:p.Arg69=
ENST00000464749.5:n.258-675G>C
ENST00000468504.5:n.302G>C
ENST00000482001.1:n.453G>C
ENST00000482847.5:n.453G>C
NM_000031.5:c.180G>C	NP_000022.3:p.Arg60=
XM_005251799.1:c.267G>C	XP_005251856.1:p.Arg89=
XM_011518363.1:c.306G>C	XP_011516665.1:p.Arg102=
XM_011518364.1:c.207G>C	XP_011516666.1:p.Arg69=
NM_001003945.2:c.267G>C	NP_001003945.1:p.Arg89=
NM_001317745.1:c.156G>C	NP_001304674.1:p.Arg52=
XM_011518364.2:c.207G>C	XP_011516666.1:p.Arg69=
XM_024447449.1:c.267G>C	XP_024303217.1:p.Arg89=
XR_002956764.1:n.680G>C
NM_000031.6:c.180G>C MANE Select	NP_000022.3:p.Arg60=
NM_001003945.3:c.267G>C	NP_001003945.1:p.Arg89=
NM_001317745.2:c.156G>C	NP_001304674.1:p.Arg52=