Canonical Allele Identifier: CA501020760

Gene: MPO

Linked Data

• MyVariant Identifiers: chr17:g.56350224A>G (hg19)

Genomic Alleles

HGVS	Genome Assembly
NC_000017.11:g.58272863A>G , CM000679.2:g.58272863A>G	GRCh38
NC_000017.10:g.56350224A>G , CM000679.1:g.56350224A>G	GRCh37
NC_000017.9:g.53705223A>G	NCBI36
NG_009629.1:g.13073T>C , LRG_84:g.13073T>C

Transcript Alleles

HGVS	Amino-acid Change
ENST00000578493.2:n.1010T>C
ENST00000699291.1:c.802T>C	ENSP00000514272.1:n.802T>C
ENST00000699292.1:n.1212T>C
ENST00000225275.4:c.1677T>C MANE Select	ENSP00000225275.3:p.Arg559=
ENST00000225275.3:c.1677T>C	ENSP00000225275.3:p.Arg559=
ENST00000577220.1:c.135T>C	ENSP00000464668.1:p.Arg45=
NM_000250.1:c.1677T>C , LRG_84t1:c.1677T>C	NP_000241.1:p.Arg559=
XM_011524821.1:c.1863T>C	XP_011523123.1:p.Arg621=
XM_011524822.1:c.1392T>C	XP_011523124.1:p.Arg464=
NM_000250.2:c.1677T>C MANE Select	NP_000241.1:p.Arg559=