Canonical Allele Identifier: CA1873365576

Gene: ALAD

Genomic Alleles

HGVS	Genome Assembly
NC_000009.12:g.113388998T= , CM000671.2:g.113388998T=	GRCh38
NC_000009.11:g.116151278T= , CM000671.1:g.116151278T=	GRCh37
NC_000009.10:g.115191099T=	NCBI36
NG_008716.1:g.17341A=

Transcript Alleles

HGVS	Amino-acid Change
ENST00000409155.8:c.910A= MANE Select	ENSP00000386284.3:p.Met304=
ENST00000409155.7:c.910A=	ENSP00000386284.3:p.Met304=
ENST00000482847.5:n.1183A=
NM_000031.5:c.910A=	NP_000022.3:p.Met304=
XM_005251799.1:c.997A=	XP_005251856.1:p.Met333=
XM_011518363.1:c.1036A=	XP_011516665.1:p.Met346=
XM_011518364.1:c.937A=	XP_011516666.1:p.Met313=
NM_001003945.2:c.997A=	NP_001003945.1:p.Met333=
NM_001317745.1:c.886A=	NP_001304674.1:p.Met296=
XM_011518364.2:c.937A=	XP_011516666.1:p.Met313=
XM_024447449.1:c.997A=	XP_024303217.1:p.Met333=
NM_000031.6:c.910A= MANE Select	NP_000022.3:p.Met304=
NM_001003945.3:c.997A=	NP_001003945.1:p.Met333=
NM_001317745.2:c.886A=	NP_001304674.1:p.Met296=