Canonical Allele Identifier: CA501023147

Gene: MPO

Linked Data

• MyVariant Identifiers: chr17:g.56350977C>T (hg19)

Genomic Alleles

HGVS	Genome Assembly
NC_000017.11:g.58273616C>T , CM000679.2:g.58273616C>T	GRCh38
NC_000017.10:g.56350977C>T , CM000679.1:g.56350977C>T	GRCh37
NC_000017.9:g.53705976C>T	NCBI36
NG_009629.1:g.12320G>A , LRG_84:g.12320G>A

Transcript Alleles

HGVS	Amino-acid Change
ENST00000578493.2:n.752G>A
ENST00000699291.1:c.544G>A	ENSP00000514272.1:p.Glu182Lys
ENST00000699292.1:n.459G>A
ENST00000225275.4:c.1419G>A MANE Select	ENSP00000225275.3:p.Arg473=
ENST00000225275.3:c.1419G>A	ENSP00000225275.3:p.Arg473=
NM_000250.1:c.1419G>A , LRG_84t1:c.1419G>A	NP_000241.1:p.Arg473=
XM_011524821.1:c.1605G>A	XP_011523123.1:p.Arg535=
XM_011524822.1:c.1134G>A	XP_011523124.1:p.Arg378=
XM_011524823.1:c.1444G>A	XP_011523125.1:p.Glu482Lys
NM_000250.2:c.1419G>A MANE Select	NP_000241.1:p.Arg473=