Canonical Allele Identifier: CA1873365572

Gene: ALAD

Genomic Alleles

HGVS	Genome Assembly
NC_000009.12:g.113388989A= , CM000671.2:g.113388989A=	GRCh38
NC_000009.11:g.116151269A= , CM000671.1:g.116151269A=	GRCh37
NC_000009.10:g.115191090A=	NCBI36
NG_008716.1:g.17350T=

Transcript Alleles

HGVS	Amino-acid Change
ENST00000409155.8:c.919T= MANE Select	ENSP00000386284.3:p.Phe307=
ENST00000409155.7:c.919T=	ENSP00000386284.3:p.Phe307=
ENST00000482847.5:n.1192T=
NM_000031.5:c.919T=	NP_000022.3:p.Phe307=
XM_005251799.1:c.1006T=	XP_005251856.1:p.Phe336=
XM_011518363.1:c.1045T=	XP_011516665.1:p.Phe349=
XM_011518364.1:c.946T=	XP_011516666.1:p.Phe316=
NM_001003945.2:c.1006T=	NP_001003945.1:p.Phe336=
NM_001317745.1:c.895T=	NP_001304674.1:p.Phe299=
XM_011518364.2:c.946T=	XP_011516666.1:p.Phe316=
XM_024447449.1:c.1006T=	XP_024303217.1:p.Phe336=
NM_000031.6:c.919T= MANE Select	NP_000022.3:p.Phe307=
NM_001003945.3:c.1006T=	NP_001003945.1:p.Phe336=
NM_001317745.2:c.895T=	NP_001304674.1:p.Phe299=