Canonical Allele Identifier: CA1873365571

Gene: ALAD

Genomic Alleles

HGVS	Genome Assembly
NC_000009.12:g.113388986G= , CM000671.2:g.113388986G=	GRCh38
NC_000009.11:g.116151266G= , CM000671.1:g.116151266G=	GRCh37
NC_000009.10:g.115191087G=	NCBI36
NG_008716.1:g.17353C=

Transcript Alleles

HGVS	Amino-acid Change
ENST00000409155.8:c.922C= MANE Select	ENSP00000386284.3:p.Arg308=
ENST00000409155.7:c.922C=	ENSP00000386284.3:p.Arg308=
ENST00000482847.5:n.1195C=
NM_000031.5:c.922C=	NP_000022.3:p.Arg308=
XM_005251799.1:c.1009C=	XP_005251856.1:p.Arg337=
XM_011518363.1:c.1048C=	XP_011516665.1:p.Arg350=
XM_011518364.1:c.949C=	XP_011516666.1:p.Arg317=
NM_001003945.2:c.1009C=	NP_001003945.1:p.Arg337=
NM_001317745.1:c.898C=	NP_001304674.1:p.Arg300=
XM_011518364.2:c.949C=	XP_011516666.1:p.Arg317=
XM_024447449.1:c.1009C=	XP_024303217.1:p.Arg337=
NM_000031.6:c.922C= MANE Select	NP_000022.3:p.Arg308=
NM_001003945.3:c.1009C=	NP_001003945.1:p.Arg337=
NM_001317745.2:c.898C=	NP_001304674.1:p.Arg300=