Canonical Allele Identifier: CA413294543

Gene: ALAS2

Linked Data

• MyVariant Identifiers: chrX:g.55044041T>C (hg19) ; chrX:g.55017608T>C (hg38)

Genomic Alleles

HGVS	Genome Assembly
NC_000023.11:g.55017608T>C , CM000685.2:g.55017608T>C	GRCh38
NC_000023.10:g.55044041T>C , CM000685.1:g.55044041T>C	GRCh37
NC_000023.9:g.55060766T>C	NCBI36
NG_008983.1:g.18457A>G

Transcript Alleles

HGVS	Amino-acid change
ENST00000650242.1:c.881A>G MANE Select	ENSP00000497236.1:p.Asn294Ser
ENST00000330807.9:c.881A>G	ENSP00000332369.5:p.Asn294Ser
ENST00000335854.8:c.770A>G	ENSP00000337131.4:p.Asn257Ser
ENST00000396198.7:c.842A>G	ENSP00000379501.3:p.Asn281Ser
ENST00000463868.5:n.598A>G
ENST00000498636.1:n.172A>G
NM_000032.4:c.881A>G	NP_000023.2:p.Asn294Ser
NM_001037967.3:c.770A>G	NP_001033056.1:p.Asn257Ser
NM_001037968.3:c.842A>G	NP_001033057.1:p.Asn281Ser
XM_005261995.2:c.953A>G	XP_005262052.1:p.Asn318Ser
XM_011530771.1:c.20A>G	XP_011529073.1:p.Asn7Ser
NM_000032.5:c.881A>G MANE Select	NP_000023.2:p.Asn294Ser
NM_001037967.4:c.770A>G	NP_001033056.1:p.Asn257Ser
NM_001037968.4:c.842A>G	NP_001033057.1:p.Asn281Ser