Canonical Allele Identifier: CA374565002

Gene: ALAD

Linked Data

• MyVariant Identifiers: chr9:g.116153830C>A (hg19) ; chr9:g.113391550C>A (hg38)

Genomic Alleles

HGVS	Genome Assembly
NC_000009.12:g.113391550C>A , CM000671.2:g.113391550C>A	GRCh38
NC_000009.11:g.116153830C>A , CM000671.1:g.116153830C>A	GRCh37
NC_000009.10:g.115193651C>A	NCBI36
NG_008716.1:g.14789G>T

Transcript Alleles

HGVS	Amino-acid Change
ENST00000409155.8:c.238G>T MANE Select	ENSP00000386284.3:p.Gly80Cys
ENST00000409155.7:c.238G>T	ENSP00000386284.3:p.Gly80Cys
ENST00000448137.5:c.265G>T	ENSP00000392748.1:p.Gly89Cys
ENST00000464749.5:n.258-617G>T
ENST00000468504.5:n.360G>T
ENST00000482001.1:n.511G>T
ENST00000482847.5:n.511G>T
NM_000031.5:c.238G>T	NP_000022.3:p.Gly80Cys
XM_005251799.1:c.325G>T	XP_005251856.1:p.Gly109Cys
XM_011518363.1:c.364G>T	XP_011516665.1:p.Gly122Cys
XM_011518364.1:c.265G>T	XP_011516666.1:p.Gly89Cys
NM_001003945.2:c.325G>T	NP_001003945.1:p.Gly109Cys
NM_001317745.1:c.214G>T	NP_001304674.1:p.Gly72Cys
XM_011518364.2:c.265G>T	XP_011516666.1:p.Gly89Cys
XM_024447449.1:c.325G>T	XP_024303217.1:p.Gly109Cys
XR_002956764.1:n.738G>T
NM_000031.6:c.238G>T MANE Select	NP_000022.3:p.Gly80Cys
NM_001003945.3:c.325G>T	NP_001003945.1:p.Gly109Cys
NM_001317745.2:c.214G>T	NP_001304674.1:p.Gly72Cys