Canonical Allele Identifier: CA1873365586

Gene: ALAD

Genomic Alleles

HGVS	Genome Assembly
NC_000009.12:g.113389021A= , CM000671.2:g.113389021A=	GRCh38
NC_000009.11:g.116151301A= , CM000671.1:g.116151301A=	GRCh37
NC_000009.10:g.115191122A=	NCBI36
NG_008716.1:g.17318T=

Transcript Alleles

HGVS	Amino-acid Change
ENST00000409155.8:c.887T= MANE Select	ENSP00000386284.3:p.Leu296=
ENST00000409155.7:c.887T=	ENSP00000386284.3:p.Leu296=
ENST00000482847.5:n.1160T=
NM_000031.5:c.887T=	NP_000022.3:p.Leu296=
XM_005251799.1:c.974T=	XP_005251856.1:p.Leu325=
XM_011518363.1:c.1013T=	XP_011516665.1:p.Leu338=
XM_011518364.1:c.914T=	XP_011516666.1:p.Leu305=
NM_001003945.2:c.974T=	NP_001003945.1:p.Leu325=
NM_001317745.1:c.863T=	NP_001304674.1:p.Leu288=
XM_011518364.2:c.914T=	XP_011516666.1:p.Leu305=
XM_024447449.1:c.974T=	XP_024303217.1:p.Leu325=
NM_000031.6:c.887T= MANE Select	NP_000022.3:p.Leu296=
NM_001003945.3:c.974T=	NP_001003945.1:p.Leu325=
NM_001317745.2:c.863T=	NP_001304674.1:p.Leu288=