Canonical Allele Identifier: CA374564956

Gene: ALAD

Linked Data

• MyVariant Identifiers: chr9:g.116153817C>G (hg19) ; chr9:g.113391537C>G (hg38)

Genomic Alleles

HGVS	Genome Assembly
NC_000009.12:g.113391537C>G , CM000671.2:g.113391537C>G	GRCh38
NC_000009.11:g.116153817C>G , CM000671.1:g.116153817C>G	GRCh37
NC_000009.10:g.115193638C>G	NCBI36
NG_008716.1:g.14802G>C

Transcript Alleles

HGVS	Amino-acid change
ENST00000409155.8:c.251G>C MANE Select	ENSP00000386284.3:p.Arg84Thr
ENST00000409155.7:c.251G>C	ENSP00000386284.3:p.Arg84Thr
ENST00000448137.5:c.278G>C	ENSP00000392748.1:p.Arg93Thr
ENST00000464749.5:n.258-604G>C
ENST00000468504.5:n.373G>C
ENST00000482001.1:n.524G>C
ENST00000482847.5:n.524G>C
NM_000031.5:c.251G>C	NP_000022.3:p.Arg84Thr
XM_005251799.1:c.338G>C	XP_005251856.1:p.Arg113Thr
XM_011518363.1:c.377G>C	XP_011516665.1:p.Arg126Thr
XM_011518364.1:c.278G>C	XP_011516666.1:p.Arg93Thr
NM_001003945.2:c.338G>C	NP_001003945.1:p.Arg113Thr
NM_001317745.1:c.227G>C	NP_001304674.1:p.Arg76Thr
XM_011518364.2:c.278G>C	XP_011516666.1:p.Arg93Thr
XM_024447449.1:c.338G>C	XP_024303217.1:p.Arg113Thr
XR_002956764.1:n.751G>C
NM_000031.6:c.251G>C MANE Select	NP_000022.3:p.Arg84Thr
NM_001003945.3:c.338G>C	NP_001003945.1:p.Arg113Thr
NM_001317745.2:c.227G>C	NP_001304674.1:p.Arg76Thr