Canonical Allele Identifier: CA2430388731

Gene: ALAS2

Genomic Alleles

HGVS	Genome Assembly
NC_000023.11:g.55009268C= , CM000685.2:g.55009268C=	GRCh38
NC_000023.10:g.55035701C= , CM000685.1:g.55035701C=	GRCh37
NC_000023.9:g.55052426C=	NCBI36
NG_008983.1:g.26797G=
NG_012568.1:g.13922C=

Transcript Alleles

HGVS	Amino-acid Change
NM_000032.5:c.1676G= MANE Select	NP_000023.2:p.Arg559=
ENST00000650242.1:c.1676G= MANE Select	ENSP00000497236.1:p.Arg559=
NM_000032.4:c.1676G=	NP_000023.2:p.Arg559=
NM_001037967.3:c.1565G=	NP_001033056.1:p.Arg522=
NM_001037967.4:c.1565G=	NP_001033056.1:p.Arg522=
NM_001037968.3:c.1637G=	NP_001033057.1:p.Arg546=
NM_001037968.4:c.1637G=	NP_001033057.1:p.Arg546=
ENST00000330807.9:c.1676G=	ENSP00000332369.5:p.Arg559=
ENST00000335854.8:c.1565G=	ENSP00000337131.4:p.Arg522=
ENST00000396198.7:c.1637G=	ENSP00000379501.3:p.Arg546=
ENST00000498636.1:n.804G=
XM_005261995.2:c.1748G=	XP_005262052.1:p.Arg583=
XM_011530771.1:c.815G=	XP_011529073.1:p.Arg272=