Canonical Allele Identifier: CA400370449

Gene: MPO

Linked Data

• MyVariant Identifiers: chr17:g.56350990G>T (hg19) ; chr17:g.58273629G>T (hg38)

Genomic Alleles

HGVS	Genome Assembly
NC_000017.11:g.58273629G>T , CM000679.2:g.58273629G>T	GRCh38
NC_000017.10:g.56350990G>T , CM000679.1:g.56350990G>T	GRCh37
NC_000017.9:g.53705989G>T	NCBI36
NG_009629.1:g.12307C>A , LRG_84:g.12307C>A

Transcript Alleles

HGVS	Amino-acid Change
ENST00000578493.2:n.739C>A
ENST00000699291.1:c.531C>A	ENSP00000514272.1:p.Ala177=
ENST00000699292.1:n.446C>A
ENST00000225275.4:c.1406C>A MANE Select	ENSP00000225275.3:p.Pro469Gln
ENST00000225275.3:c.1406C>A	ENSP00000225275.3:p.Pro469Gln
NM_000250.1:c.1406C>A , LRG_84t1:c.1406C>A	NP_000241.1:p.Pro469Gln
XM_011524821.1:c.1592C>A	XP_011523123.1:p.Pro531Gln
XM_011524822.1:c.1121C>A	XP_011523124.1:p.Pro374Gln
XM_011524823.1:c.1431C>A	XP_011523125.1:p.Ala477=
NM_000250.2:c.1406C>A MANE Select	NP_000241.1:p.Pro469Gln