Canonical Allele Identifier: CA374563045

Gene: ALAD

Linked Data

• COSMIC: COSM3699352 ; COSM3699353
• MyVariant Identifiers: chr9:g.116151329G>A (hg19) ; chr9:g.113389049G>A (hg38)

Genomic Alleles

HGVS	Genome Assembly
NC_000009.12:g.113389049G>A , CM000671.2:g.113389049G>A	GRCh38
NC_000009.11:g.116151329G>A , CM000671.1:g.116151329G>A	GRCh37
NC_000009.10:g.115191150G>A	NCBI36
NG_008716.1:g.17290C>T

Transcript Alleles

HGVS	Amino-acid Change
ENST00000409155.8:c.859C>T MANE Select	ENSP00000386284.3:p.His287Tyr
ENST00000409155.7:c.859C>T	ENSP00000386284.3:p.His287Tyr
ENST00000482847.5:n.1132C>T
NM_000031.5:c.859C>T	NP_000022.3:p.His287Tyr
XM_005251799.1:c.946C>T	XP_005251856.1:p.His316Tyr
XM_011518363.1:c.985C>T	XP_011516665.1:p.His329Tyr
XM_011518364.1:c.886C>T	XP_011516666.1:p.His296Tyr
NM_001003945.2:c.946C>T	NP_001003945.1:p.His316Tyr
NM_001317745.1:c.835C>T	NP_001304674.1:p.His279Tyr
XM_011518364.2:c.886C>T	XP_011516666.1:p.His296Tyr
XM_024447449.1:c.946C>T	XP_024303217.1:p.His316Tyr
NM_000031.6:c.859C>T MANE Select	NP_000022.3:p.His287Tyr
NM_001003945.3:c.946C>T	NP_001003945.1:p.His316Tyr
NM_001317745.2:c.835C>T	NP_001304674.1:p.His279Tyr