Canonical Allele Identifier: CA413295440

Gene: ALAS2

Linked Data

• MyVariant Identifiers: chrX:g.55047526G>T (hg19) ; chrX:g.55021093G>T (hg38)

Genomic Alleles

HGVS	Genome Assembly
NC_000023.11:g.55021093G>T , CM000685.2:g.55021093G>T	GRCh38
NC_000023.10:g.55047526G>T , CM000685.1:g.55047526G>T	GRCh37
NC_000023.9:g.55064251G>T	NCBI36
NG_008983.1:g.14972C>A

Transcript Alleles

HGVS	Amino-acid Change
ENST00000455688.2:c.381C>A	ENSP00000407204.2:p.Tyr127Ter
ENST00000477869.6:c.270C>A	ENSP00000496725.1:p.Tyr90Ter
ENST00000493869.2:c.305-589C>A	ENSP00000495713.1:n.305-589C>A
ENST00000650242.1:c.597C>A MANE Select	ENSP00000497236.1:p.Tyr199Ter
ENST00000330807.9:c.597C>A	ENSP00000332369.5:p.Tyr199Ter
ENST00000335854.8:c.486C>A	ENSP00000337131.4:p.Tyr162Ter
ENST00000396198.7:c.558C>A	ENSP00000379501.3:p.Tyr186Ter
ENST00000455688.1:c.452C>A
ENST00000463868.5:n.356-589C>A
ENST00000477869.5:n.341C>A
ENST00000493869.1:n.537C>A
NM_000032.4:c.597C>A	NP_000023.2:p.Tyr199Ter
NM_001037967.3:c.486C>A	NP_001033056.1:p.Tyr162Ter
NM_001037968.3:c.558C>A	NP_001033057.1:p.Tyr186Ter
XM_005261995.2:c.669C>A	XP_005262052.1:p.Tyr223Ter
XM_011530771.1:c.-223-589C>A	XP_011529073.1:n.-223-589C>A
NM_000032.5:c.597C>A MANE Select	NP_000023.2:p.Tyr199Ter
NM_001037967.4:c.486C>A	NP_001033056.1:p.Tyr162Ter
NM_001037968.4:c.558C>A	NP_001033057.1:p.Tyr186Ter