Canonical Allele Identifier: CA374564996

Gene: ALAD

Linked Data

• MyVariant Identifiers: chr9:g.116153829C>A (hg19) ; chr9:g.113391549C>A (hg38)

Genomic Alleles

HGVS	Genome Assembly
NC_000009.12:g.113391549C>A , CM000671.2:g.113391549C>A	GRCh38
NC_000009.11:g.116153829C>A , CM000671.1:g.116153829C>A	GRCh37
NC_000009.10:g.115193650C>A	NCBI36
NG_008716.1:g.14790G>T

Transcript Alleles

HGVS	Amino-acid change
ENST00000409155.8:c.239G>T MANE Select	ENSP00000386284.3:p.Gly80Val
ENST00000409155.7:c.239G>T	ENSP00000386284.3:p.Gly80Val
ENST00000448137.5:c.266G>T	ENSP00000392748.1:p.Gly89Val
ENST00000464749.5:n.258-616G>T
ENST00000468504.5:n.361G>T
ENST00000482001.1:n.512G>T
ENST00000482847.5:n.512G>T
NM_000031.5:c.239G>T	NP_000022.3:p.Gly80Val
XM_005251799.1:c.326G>T	XP_005251856.1:p.Gly109Val
XM_011518363.1:c.365G>T	XP_011516665.1:p.Gly122Val
XM_011518364.1:c.266G>T	XP_011516666.1:p.Gly89Val
NM_001003945.2:c.326G>T	NP_001003945.1:p.Gly109Val
NM_001317745.1:c.215G>T	NP_001304674.1:p.Gly72Val
XM_011518364.2:c.266G>T	XP_011516666.1:p.Gly89Val
XM_024447449.1:c.326G>T	XP_024303217.1:p.Gly109Val
XR_002956764.1:n.739G>T
NM_000031.6:c.239G>T MANE Select	NP_000022.3:p.Gly80Val
NM_001003945.3:c.326G>T	NP_001003945.1:p.Gly109Val
NM_001317745.2:c.215G>T	NP_001304674.1:p.Gly72Val