Canonical Allele Identifier: CA1873365593

Gene: ALAD

Genomic Alleles

HGVS	Genome Assembly
NC_000009.12:g.113389035G= , CM000671.2:g.113389035G=	GRCh38
NC_000009.11:g.116151315G= , CM000671.1:g.116151315G=	GRCh37
NC_000009.10:g.115191136G=	NCBI36
NG_008716.1:g.17304C=

Transcript Alleles

HGVS	Amino-acid Change
ENST00000409155.8:c.873C= MANE Select	ENSP00000386284.3:p.Ala291=
ENST00000409155.7:c.873C=	ENSP00000386284.3:p.Ala291=
ENST00000482847.5:n.1146C=
NM_000031.5:c.873C=	NP_000022.3:p.Ala291=
XM_005251799.1:c.960C=	XP_005251856.1:p.Ala320=
XM_011518363.1:c.999C=	XP_011516665.1:p.Ala333=
XM_011518364.1:c.900C=	XP_011516666.1:p.Ala300=
NM_001003945.2:c.960C=	NP_001003945.1:p.Ala320=
NM_001317745.1:c.849C=	NP_001304674.1:p.Ala283=
XM_011518364.2:c.900C=	XP_011516666.1:p.Ala300=
XM_024447449.1:c.960C=	XP_024303217.1:p.Ala320=
NM_000031.6:c.873C= MANE Select	NP_000022.3:p.Ala291=
NM_001003945.3:c.960C=	NP_001003945.1:p.Ala320=
NM_001317745.2:c.849C=	NP_001304674.1:p.Ala283=