Canonical Allele Identifier: CA516580832

Gene: ALAS2

Linked Data

• MyVariant Identifiers: chrX:g.55035679G>T (hg19)

Genomic Alleles

HGVS	Genome Assembly
NC_000023.11:g.55009246G>T , CM000685.2:g.55009246G>T	GRCh38
NC_000023.10:g.55035679G>T , CM000685.1:g.55035679G>T	GRCh37
NC_000023.9:g.55052404G>T	NCBI36
NG_008983.1:g.26819C>A
NG_012568.1:g.13900G>T

Transcript Alleles

HGVS	Amino-acid Change
ENST00000650242.1:c.1698C>A MANE Select	ENSP00000497236.1:p.Leu566=
ENST00000330807.9:c.1698C>A	ENSP00000332369.5:p.Leu566=
ENST00000335854.8:c.1587C>A	ENSP00000337131.4:p.Leu529=
ENST00000396198.7:c.1659C>A	ENSP00000379501.3:p.Leu553=
ENST00000498636.1:n.826C>A
NM_000032.4:c.1698C>A	NP_000023.2:p.Leu566=
NM_001037967.3:c.1587C>A	NP_001033056.1:p.Leu529=
NM_001037968.3:c.1659C>A	NP_001033057.1:p.Leu553=
XM_005261995.2:c.1770C>A	XP_005262052.1:p.Leu590=
XM_011530771.1:c.837C>A	XP_011529073.1:p.Leu279=
NM_000032.5:c.1698C>A MANE Select	NP_000023.2:p.Leu566=
NM_001037967.4:c.1587C>A	NP_001033056.1:p.Leu529=
NM_001037968.4:c.1659C>A	NP_001033057.1:p.Leu553=