Canonical Allele Identifier: CA501020617

Gene: MPO

Linked Data

• MyVariant Identifiers: chr17:g.56350196G>T (hg19)

Genomic Alleles

HGVS	Genome Assembly
NC_000017.11:g.58272835G>T , CM000679.2:g.58272835G>T	GRCh38
NC_000017.10:g.56350196G>T , CM000679.1:g.56350196G>T	GRCh37
NC_000017.9:g.53705195G>T	NCBI36
NG_009629.1:g.13101C>A , LRG_84:g.13101C>A

Transcript Alleles

HGVS	Amino-acid change
ENST00000578493.2:n.1038C>A
ENST00000699291.1:c.830C>A	ENSP00000514272.1:n.830C>A
ENST00000699292.1:n.1240C>A
ENST00000225275.4:c.1705C>A MANE Select	ENSP00000225275.3:p.Arg569=
ENST00000225275.3:c.1705C>A	ENSP00000225275.3:p.Arg569=
ENST00000577220.1:c.163C>A	ENSP00000464668.1:p.Arg55=
NM_000250.1:c.1705C>A , LRG_84t1:c.1705C>A	NP_000241.1:p.Arg569=
XM_011524821.1:c.1891C>A	XP_011523123.1:p.Arg631=
XM_011524822.1:c.1420C>A	XP_011523124.1:p.Arg474=
NM_000250.2:c.1705C>A MANE Select	NP_000241.1:p.Arg569=