Canonical Allele Identifier: CA466758201

Gene: ALAD

Linked Data

• MyVariant Identifiers: chr9:g.116153818T>G (hg19)

Genomic Alleles

HGVS	Genome Assembly
NC_000009.12:g.113391538T>G , CM000671.2:g.113391538T>G	GRCh38
NC_000009.11:g.116153818T>G , CM000671.1:g.116153818T>G	GRCh37
NC_000009.10:g.115193639T>G	NCBI36
NG_008716.1:g.14801A>C

Transcript Alleles

HGVS	Amino-acid change
ENST00000409155.8:c.250A>C MANE Select	ENSP00000386284.3:p.Arg84=
ENST00000409155.7:c.250A>C	ENSP00000386284.3:p.Arg84=
ENST00000448137.5:c.277A>C	ENSP00000392748.1:p.Arg93=
ENST00000464749.5:n.258-605A>C
ENST00000468504.5:n.372A>C
ENST00000482001.1:n.523A>C
ENST00000482847.5:n.523A>C
NM_000031.5:c.250A>C	NP_000022.3:p.Arg84=
XM_005251799.1:c.337A>C	XP_005251856.1:p.Arg113=
XM_011518363.1:c.376A>C	XP_011516665.1:p.Arg126=
XM_011518364.1:c.277A>C	XP_011516666.1:p.Arg93=
NM_001003945.2:c.337A>C	NP_001003945.1:p.Arg113=
NM_001317745.1:c.226A>C	NP_001304674.1:p.Arg76=
XM_011518364.2:c.277A>C	XP_011516666.1:p.Arg93=
XM_024447449.1:c.337A>C	XP_024303217.1:p.Arg113=
XR_002956764.1:n.750A>C
NM_000031.6:c.250A>C MANE Select	NP_000022.3:p.Arg84=
NM_001003945.3:c.337A>C	NP_001003945.1:p.Arg113=
NM_001317745.2:c.226A>C	NP_001304674.1:p.Arg76=