Canonical Allele Identifier: CA413293330

Gene: ALAS2

Linked Data

• MyVariant Identifiers: chrX:g.55042019C>A (hg19) ; chrX:g.55015586C>A (hg38)

Genomic Alleles

HGVS	Genome Assembly
NC_000023.11:g.55015586C>A , CM000685.2:g.55015586C>A	GRCh38
NC_000023.10:g.55042019C>A , CM000685.1:g.55042019C>A	GRCh37
NC_000023.9:g.55058744C>A	NCBI36
NG_008983.1:g.20479G>T

Transcript Alleles

HGVS	Amino-acid Change
ENST00000650242.1:c.1160G>T MANE Select	ENSP00000497236.1:p.Gly387Val
ENST00000330807.9:c.1160G>T	ENSP00000332369.5:p.Gly387Val
ENST00000335854.8:c.1049G>T	ENSP00000337131.4:p.Gly350Val
ENST00000396198.7:c.1121G>T	ENSP00000379501.3:p.Gly374Val
ENST00000498636.1:n.451G>T
NM_000032.4:c.1160G>T	NP_000023.2:p.Gly387Val
NM_001037967.3:c.1049G>T	NP_001033056.1:p.Gly350Val
NM_001037968.3:c.1121G>T	NP_001033057.1:p.Gly374Val
XM_005261995.2:c.1232G>T	XP_005262052.1:p.Gly411Val
XM_011530771.1:c.299G>T	XP_011529073.1:p.Gly100Val
NM_000032.5:c.1160G>T MANE Select	NP_000023.2:p.Gly387Val
NM_001037967.4:c.1049G>T	NP_001033056.1:p.Gly350Val
NM_001037968.4:c.1121G>T	NP_001033057.1:p.Gly374Val