Canonical Allele Identifier: CA413293327

Gene: ALAS2

Linked Data

• MyVariant Identifiers: chrX:g.55042017T>A (hg19) ; chrX:g.55015584T>A (hg38)

Genomic Alleles

HGVS	Genome Assembly
NC_000023.11:g.55015584T>A , CM000685.2:g.55015584T>A	GRCh38
NC_000023.10:g.55042017T>A , CM000685.1:g.55042017T>A	GRCh37
NC_000023.9:g.55058742T>A	NCBI36
NG_008983.1:g.20481A>T

Transcript Alleles

HGVS	Amino-acid Change
ENST00000650242.1:c.1162A>T MANE Select	ENSP00000497236.1:p.Thr388Ser
ENST00000330807.9:c.1162A>T	ENSP00000332369.5:p.Thr388Ser
ENST00000335854.8:c.1051A>T	ENSP00000337131.4:p.Thr351Ser
ENST00000396198.7:c.1123A>T	ENSP00000379501.3:p.Thr375Ser
ENST00000498636.1:n.453A>T
NM_000032.4:c.1162A>T	NP_000023.2:p.Thr388Ser
NM_001037967.3:c.1051A>T	NP_001033056.1:p.Thr351Ser
NM_001037968.3:c.1123A>T	NP_001033057.1:p.Thr375Ser
XM_005261995.2:c.1234A>T	XP_005262052.1:p.Thr412Ser
XM_011530771.1:c.301A>T	XP_011529073.1:p.Thr101Ser
NM_000032.5:c.1162A>T MANE Select	NP_000023.2:p.Thr388Ser
NM_001037967.4:c.1051A>T	NP_001033056.1:p.Thr351Ser
NM_001037968.4:c.1123A>T	NP_001033057.1:p.Thr375Ser