Canonical Allele Identifier: CA413293320

Gene: ALAS2

Linked Data

• MyVariant Identifiers: chrX:g.55042013A>G (hg19) ; chrX:g.55015580A>G (hg38)

Genomic Alleles

HGVS	Genome Assembly
NC_000023.11:g.55015580A>G , CM000685.2:g.55015580A>G	GRCh38
NC_000023.10:g.55042013A>G , CM000685.1:g.55042013A>G	GRCh37
NC_000023.9:g.55058738A>G	NCBI36
NG_008983.1:g.20485T>C

Transcript Alleles

HGVS	Amino-acid Change
ENST00000650242.1:c.1166T>C MANE Select	ENSP00000497236.1:p.Leu389Pro
ENST00000330807.9:c.1166T>C	ENSP00000332369.5:p.Leu389Pro
ENST00000335854.8:c.1055T>C	ENSP00000337131.4:p.Leu352Pro
ENST00000396198.7:c.1127T>C	ENSP00000379501.3:p.Leu376Pro
ENST00000498636.1:n.457T>C
NM_000032.4:c.1166T>C	NP_000023.2:p.Leu389Pro
NM_001037967.3:c.1055T>C	NP_001033056.1:p.Leu352Pro
NM_001037968.3:c.1127T>C	NP_001033057.1:p.Leu376Pro
XM_005261995.2:c.1238T>C	XP_005262052.1:p.Leu413Pro
XM_011530771.1:c.305T>C	XP_011529073.1:p.Leu102Pro
NM_000032.5:c.1166T>C MANE Select	NP_000023.2:p.Leu389Pro
NM_001037967.4:c.1055T>C	NP_001033056.1:p.Leu352Pro
NM_001037968.4:c.1127T>C	NP_001033057.1:p.Leu376Pro