Canonical Allele Identifier: CA1873365587

Gene: ALAD

Genomic Alleles

HGVS	Genome Assembly
NC_000009.12:g.113389026A= , CM000671.2:g.113389026A=	GRCh38
NC_000009.11:g.116151306A= , CM000671.1:g.116151306A=	GRCh37
NC_000009.10:g.115191127A=	NCBI36
NG_008716.1:g.17313T=

Transcript Alleles

HGVS	Amino-acid Change
ENST00000409155.8:c.882T= MANE Select	ENSP00000386284.3:p.Phe294=
ENST00000409155.7:c.882T=	ENSP00000386284.3:p.Phe294=
ENST00000482847.5:n.1155T=
NM_000031.5:c.882T=	NP_000022.3:p.Phe294=
XM_005251799.1:c.969T=	XP_005251856.1:p.Phe323=
XM_011518363.1:c.1008T=	XP_011516665.1:p.Phe336=
XM_011518364.1:c.909T=	XP_011516666.1:p.Phe303=
NM_001003945.2:c.969T=	NP_001003945.1:p.Phe323=
NM_001317745.1:c.858T=	NP_001304674.1:p.Phe286=
XM_011518364.2:c.909T=	XP_011516666.1:p.Phe303=
XM_024447449.1:c.969T=	XP_024303217.1:p.Phe323=
NM_000031.6:c.882T= MANE Select	NP_000022.3:p.Phe294=
NM_001003945.3:c.969T=	NP_001003945.1:p.Phe323=
NM_001317745.2:c.858T=	NP_001304674.1:p.Phe286=