Canonical Allele Identifier: CA400368985

Gene: MPO

Linked Data

• ClinVar Variation Id: 3202580
• ClinVar RCV Id: RCV004495976
• dbSNP Id: rs1970383257
• MyVariant Identifiers: chr17:g.56350121G>A (hg19) ; chr17:g.58272760G>A (hg38)

Genomic Alleles

HGVS	Genome Assembly
NC_000017.11:g.58272760G>A , CM000679.2:g.58272760G>A	GRCh38
NC_000017.10:g.56350121G>A , CM000679.1:g.56350121G>A	GRCh37
NC_000017.9:g.53705120G>A	NCBI36
NG_009629.1:g.13176C>T , LRG_84:g.13176C>T

Transcript Alleles

HGVS	Amino-acid Change
ENST00000578493.2:n.1113C>T
ENST00000699291.1:c.905C>T	ENSP00000514272.1:n.905C>T
ENST00000699292.1:n.1315C>T
ENST00000225275.4:c.1780C>T MANE Select	ENSP00000225275.3:p.His594Tyr
ENST00000225275.3:c.1780C>T	ENSP00000225275.3:p.His594Tyr
ENST00000577220.1:c.183+55C>T	ENSP00000464668.1:n.183+55C>T
NM_000250.1:c.1780C>T , LRG_84t1:c.1780C>T	NP_000241.1:p.His594Tyr
XM_011524821.1:c.1966C>T	XP_011523123.1:p.His656Tyr
XM_011524822.1:c.1495C>T	XP_011523124.1:p.His499Tyr
NM_000250.2:c.1780C>T MANE Select	NP_000241.1:p.His594Tyr