Canonical Allele Identifier: CA1873366758

Gene: ALAD

Genomic Alleles

HGVS	Genome Assembly
NC_000009.12:g.113391597A= , CM000671.2:g.113391597A=	GRCh38
NC_000009.11:g.116153877A= , CM000671.1:g.116153877A=	GRCh37
NC_000009.10:g.115193698A=	NCBI36
NG_008716.1:g.14742T=

Transcript Alleles

HGVS	Amino-acid Change
ENST00000409155.8:c.191T= MANE Select	ENSP00000386284.3:p.Met64=
ENST00000409155.7:c.191T=	ENSP00000386284.3:p.Met64=
ENST00000448137.5:c.218T=	ENSP00000392748.1:p.Met73=
ENST00000464749.5:n.258-664T=
ENST00000468504.5:n.313T=
ENST00000482001.1:n.464T=
ENST00000482847.5:n.464T=
NM_000031.5:c.191T=	NP_000022.3:p.Met64=
XM_005251799.1:c.278T=	XP_005251856.1:p.Met93=
XM_011518363.1:c.317T=	XP_011516665.1:p.Met106=
XM_011518364.1:c.218T=	XP_011516666.1:p.Met73=
NM_001003945.2:c.278T=	NP_001003945.1:p.Met93=
NM_001317745.1:c.167T=	NP_001304674.1:p.Met56=
XM_011518364.2:c.218T=	XP_011516666.1:p.Met73=
XM_024447449.1:c.278T=	XP_024303217.1:p.Met93=
XR_002956764.1:n.691T=
NM_000031.6:c.191T= MANE Select	NP_000022.3:p.Met64=
NM_001003945.3:c.278T=	NP_001003945.1:p.Met93=
NM_001317745.2:c.167T=	NP_001304674.1:p.Met56=