Canonical Allele Identifier: CA374562995

Gene: ALAD

Linked Data

• MyVariant Identifiers: chr9:g.116151304T>G (hg19) ; chr9:g.113389024T>G (hg38)

Genomic Alleles

HGVS	Genome Assembly
NC_000009.12:g.113389024T>G , CM000671.2:g.113389024T>G	GRCh38
NC_000009.11:g.116151304T>G , CM000671.1:g.116151304T>G	GRCh37
NC_000009.10:g.115191125T>G	NCBI36
NG_008716.1:g.17315A>C

Transcript Alleles

HGVS	Amino-acid Change
ENST00000409155.8:c.884A>C MANE Select	ENSP00000386284.3:p.Asp295Ala
ENST00000409155.7:c.884A>C	ENSP00000386284.3:p.Asp295Ala
ENST00000482847.5:n.1157A>C
NM_000031.5:c.884A>C	NP_000022.3:p.Asp295Ala
XM_005251799.1:c.971A>C	XP_005251856.1:p.Asp324Ala
XM_011518363.1:c.1010A>C	XP_011516665.1:p.Asp337Ala
XM_011518364.1:c.911A>C	XP_011516666.1:p.Asp304Ala
NM_001003945.2:c.971A>C	NP_001003945.1:p.Asp324Ala
NM_001317745.1:c.860A>C	NP_001304674.1:p.Asp287Ala
XM_011518364.2:c.911A>C	XP_011516666.1:p.Asp304Ala
XM_024447449.1:c.971A>C	XP_024303217.1:p.Asp324Ala
NM_000031.6:c.884A>C MANE Select	NP_000022.3:p.Asp295Ala
NM_001003945.3:c.971A>C	NP_001003945.1:p.Asp324Ala
NM_001317745.2:c.860A>C	NP_001304674.1:p.Asp287Ala