Canonical Allele Identifier: CA374565004

Gene: ALAD

Linked Data

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

Genomic Alleles

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

Transcript Alleles

HGVS	Amino-acid Change
ENST00000409155.8:c.238G>C MANE Select	ENSP00000386284.3:p.Gly80Arg
ENST00000409155.7:c.238G>C	ENSP00000386284.3:p.Gly80Arg
ENST00000448137.5:c.265G>C	ENSP00000392748.1:p.Gly89Arg
ENST00000464749.5:n.258-617G>C
ENST00000468504.5:n.360G>C
ENST00000482001.1:n.511G>C
ENST00000482847.5:n.511G>C
NM_000031.5:c.238G>C	NP_000022.3:p.Gly80Arg
XM_005251799.1:c.325G>C	XP_005251856.1:p.Gly109Arg
XM_011518363.1:c.364G>C	XP_011516665.1:p.Gly122Arg
XM_011518364.1:c.265G>C	XP_011516666.1:p.Gly89Arg
NM_001003945.2:c.325G>C	NP_001003945.1:p.Gly109Arg
NM_001317745.1:c.214G>C	NP_001304674.1:p.Gly72Arg
XM_011518364.2:c.265G>C	XP_011516666.1:p.Gly89Arg
XM_024447449.1:c.325G>C	XP_024303217.1:p.Gly109Arg
XR_002956764.1:n.738G>C
NM_000031.6:c.238G>C MANE Select	NP_000022.3:p.Gly80Arg
NM_001003945.3:c.325G>C	NP_001003945.1:p.Gly109Arg
NM_001317745.2:c.214G>C	NP_001304674.1:p.Gly72Arg