Canonical Allele Identifier: CA2430391397

Gene: ALAS2

Genomic Alleles

HGVS	Genome Assembly
NC_000023.11:g.55017603C= , CM000685.2:g.55017603C=	GRCh38
NC_000023.10:g.55044036C= , CM000685.1:g.55044036C=	GRCh37
NC_000023.9:g.55060761C=	NCBI36
NG_008983.1:g.18462G=

Transcript Alleles

HGVS	Amino-acid change
ENST00000650242.1:c.886G= MANE Select	ENSP00000497236.1:p.Gly296=
ENST00000330807.9:c.886G=	ENSP00000332369.5:p.Gly296=
ENST00000335854.8:c.775G=	ENSP00000337131.4:p.Gly259=
ENST00000396198.7:c.847G=	ENSP00000379501.3:p.Gly283=
ENST00000463868.5:n.603G=
ENST00000498636.1:n.177G=
NM_000032.4:c.886G=	NP_000023.2:p.Gly296=
NM_001037967.3:c.775G=	NP_001033056.1:p.Gly259=
NM_001037968.3:c.847G=	NP_001033057.1:p.Gly283=
XM_005261995.2:c.958G=	XP_005262052.1:p.Gly320=
XM_011530771.1:c.25G=	XP_011529073.1:p.Gly9=
NM_000032.5:c.886G= MANE Select	NP_000023.2:p.Gly296=
NM_001037967.4:c.775G=	NP_001033056.1:p.Gly259=
NM_001037968.4:c.847G=	NP_001033057.1:p.Gly283=