Canonical Allele Identifier: CA374562989

Gene: ALAD

Linked Data

• MyVariant Identifiers: chr9:g.116151302G>C (hg19) ; chr9:g.113389022G>C (hg38)

Genomic Alleles

HGVS	Genome Assembly
NC_000009.12:g.113389022G>C , CM000671.2:g.113389022G>C	GRCh38
NC_000009.11:g.116151302G>C , CM000671.1:g.116151302G>C	GRCh37
NC_000009.10:g.115191123G>C	NCBI36
NG_008716.1:g.17317C>G

Transcript Alleles

HGVS	Amino-acid Change
ENST00000409155.8:c.886C>G MANE Select	ENSP00000386284.3:p.Leu296Val
ENST00000409155.7:c.886C>G	ENSP00000386284.3:p.Leu296Val
ENST00000482847.5:n.1159C>G
NM_000031.5:c.886C>G	NP_000022.3:p.Leu296Val
XM_005251799.1:c.973C>G	XP_005251856.1:p.Leu325Val
XM_011518363.1:c.1012C>G	XP_011516665.1:p.Leu338Val
XM_011518364.1:c.913C>G	XP_011516666.1:p.Leu305Val
NM_001003945.2:c.973C>G	NP_001003945.1:p.Leu325Val
NM_001317745.1:c.862C>G	NP_001304674.1:p.Leu288Val
XM_011518364.2:c.913C>G	XP_011516666.1:p.Leu305Val
XM_024447449.1:c.973C>G	XP_024303217.1:p.Leu325Val
NM_000031.6:c.886C>G MANE Select	NP_000022.3:p.Leu296Val
NM_001003945.3:c.973C>G	NP_001003945.1:p.Leu325Val
NM_001317745.2:c.862C>G	NP_001304674.1:p.Leu288Val