Canonical Allele Identifier: CA501020680

Gene: MPO

Linked Data

• MyVariant Identifiers: chr17:g.56350209T>A (hg19)

Genomic Alleles

HGVS	Genome Assembly
NC_000017.11:g.58272848T>A , CM000679.2:g.58272848T>A	GRCh38
NC_000017.10:g.56350209T>A , CM000679.1:g.56350209T>A	GRCh37
NC_000017.9:g.53705208T>A	NCBI36
NG_009629.1:g.13088A>T , LRG_84:g.13088A>T

Transcript Alleles

HGVS	Amino-acid change
ENST00000578493.2:n.1025A>T
ENST00000699291.1:c.817A>T	ENSP00000514272.1:n.817A>T
ENST00000699292.1:n.1227A>T
ENST00000225275.4:c.1692A>T MANE Select	ENSP00000225275.3:p.Ala564=
ENST00000225275.3:c.1692A>T	ENSP00000225275.3:p.Ala564=
ENST00000577220.1:c.150A>T	ENSP00000464668.1:p.Ala50=
NM_000250.1:c.1692A>T , LRG_84t1:c.1692A>T	NP_000241.1:p.Ala564=
XM_011524821.1:c.1878A>T	XP_011523123.1:p.Ala626=
XM_011524822.1:c.1407A>T	XP_011523124.1:p.Ala469=
NM_000250.2:c.1692A>T MANE Select	NP_000241.1:p.Ala564=