Canonical Allele Identifier: CA374565046

Gene: ALAD

Linked Data

• MyVariant Identifiers: chr9:g.116153839A>T (hg19) ; chr9:g.113391559A>T (hg38)

Genomic Alleles

HGVS	Genome Assembly
NC_000009.12:g.113391559A>T , CM000671.2:g.113391559A>T	GRCh38
NC_000009.11:g.116153839A>T , CM000671.1:g.116153839A>T	GRCh37
NC_000009.10:g.115193660A>T	NCBI36
NG_008716.1:g.14780T>A

Transcript Alleles

HGVS	Amino-acid Change
ENST00000409155.8:c.229T>A MANE Select	ENSP00000386284.3:p.Leu77Met
ENST00000409155.7:c.229T>A	ENSP00000386284.3:p.Leu77Met
ENST00000448137.5:c.256T>A	ENSP00000392748.1:p.Leu86Met
ENST00000464749.5:n.258-626T>A
ENST00000468504.5:n.351T>A
ENST00000482001.1:n.502T>A
ENST00000482847.5:n.502T>A
NM_000031.5:c.229T>A	NP_000022.3:p.Leu77Met
XM_005251799.1:c.316T>A	XP_005251856.1:p.Leu106Met
XM_011518363.1:c.355T>A	XP_011516665.1:p.Leu119Met
XM_011518364.1:c.256T>A	XP_011516666.1:p.Leu86Met
NM_001003945.2:c.316T>A	NP_001003945.1:p.Leu106Met
NM_001317745.1:c.205T>A	NP_001304674.1:p.Leu69Met
XM_011518364.2:c.256T>A	XP_011516666.1:p.Leu86Met
XM_024447449.1:c.316T>A	XP_024303217.1:p.Leu106Met
XR_002956764.1:n.729T>A
NM_000031.6:c.229T>A MANE Select	NP_000022.3:p.Leu77Met
NM_001003945.3:c.316T>A	NP_001003945.1:p.Leu106Met
NM_001317745.2:c.205T>A	NP_001304674.1:p.Leu69Met