Canonical Allele Identifier: CA1873365616

Gene: ALAD

Genomic Alleles

HGVS	Genome Assembly
NC_000009.12:g.113389088C= , CM000671.2:g.113389088C=	GRCh38
NC_000009.11:g.116151368C= , CM000671.1:g.116151368C=	GRCh37
NC_000009.10:g.115191189C=	NCBI36
NG_008716.1:g.17251G=

Transcript Alleles

HGVS	Amino-acid Change
NM_000031.6:c.820G= MANE Select	NP_000022.3:p.Ala274=
ENST00000409155.8:c.820G= MANE Select	ENSP00000386284.3:p.Ala274=
NM_000031.5:c.820G=	NP_000022.3:p.Ala274=
NM_001003945.2:c.907G=	NP_001003945.1:p.Ala303=
NM_001003945.3:c.907G=	NP_001003945.1:p.Ala303=
NM_001317745.1:c.796G=	NP_001304674.1:p.Ala266=
NM_001317745.2:c.796G=	NP_001304674.1:p.Ala266=
ENST00000409155.7:c.820G=	ENSP00000386284.3:p.Ala274=
ENST00000482847.5:n.1093G=
XM_005251799.1:c.907G=	XP_005251856.1:p.Ala303=
XM_011518363.1:c.946G=	XP_011516665.1:p.Ala316=
XM_011518364.1:c.847G=	XP_011516666.1:p.Ala283=
XM_011518364.2:c.847G=	XP_011516666.1:p.Ala283=
XM_024447449.1:c.907G=	XP_024303217.1:p.Ala303=