Canonical Allele Identifier: CA1873366403

Gene: ALAD

Genomic Alleles

HGVS	Genome Assembly
NC_000009.12:g.113390798C= , CM000671.2:g.113390798C=	GRCh38
NC_000009.11:g.116153078C= , CM000671.1:g.116153078C=	GRCh37
NC_000009.10:g.115192899C=	NCBI36
NG_008716.1:g.15541G=

Transcript Alleles

HGVS	Amino-acid Change
NM_000031.6:c.397G= MANE Select	NP_000022.3:p.Gly133=
ENST00000409155.8:c.397G= MANE Select	ENSP00000386284.3:p.Gly133=
NM_000031.5:c.397G=	NP_000022.3:p.Gly133=
NM_001003945.2:c.484G=	NP_001003945.1:p.Gly162=
NM_001003945.3:c.484G=	NP_001003945.1:p.Gly162=
NM_001317745.1:c.373G=	NP_001304674.1:p.Gly125=
NM_001317745.2:c.373G=	NP_001304674.1:p.Gly125=
ENST00000409155.7:c.397G=	ENSP00000386284.3:p.Gly133=
ENST00000464749.5:n.393G=
ENST00000468504.5:n.519G=
ENST00000482847.5:n.670G=
XM_005251799.1:c.484G=	XP_005251856.1:p.Gly162=
XM_011518363.1:c.523G=	XP_011516665.1:p.Gly175=
XM_011518364.1:c.424G=	XP_011516666.1:p.Gly142=
XM_011518364.2:c.424G=	XP_011516666.1:p.Gly142=
XM_024447449.1:c.484G=	XP_024303217.1:p.Gly162=
XR_002956764.1:n.897G=