Canonical Allele Identifier: CA400370490

Gene: MPO

Linked Data

• MyVariant Identifiers: chr17:g.56351005G>T (hg19) ; chr17:g.58273644G>T (hg38)

Genomic Alleles

HGVS	Genome Assembly
NC_000017.11:g.58273644G>T , CM000679.2:g.58273644G>T	GRCh38
NC_000017.10:g.56351005G>T , CM000679.1:g.56351005G>T	GRCh37
NC_000017.9:g.53706004G>T	NCBI36
NG_009629.1:g.12292C>A , LRG_84:g.12292C>A

Transcript Alleles

HGVS	Amino-acid Change
ENST00000578493.2:n.724C>A
ENST00000699291.1:c.516C>A	ENSP00000514272.1:p.Ala172=
ENST00000699292.1:n.431C>A
ENST00000225275.4:c.1391C>A MANE Select	ENSP00000225275.3:p.Pro464His
ENST00000225275.3:c.1391C>A	ENSP00000225275.3:p.Pro464His
NM_000250.1:c.1391C>A , LRG_84t1:c.1391C>A	NP_000241.1:p.Pro464His
XM_011524821.1:c.1577C>A	XP_011523123.1:p.Pro526His
XM_011524822.1:c.1106C>A	XP_011523124.1:p.Pro369His
XM_011524823.1:c.1416C>A	XP_011523125.1:p.Ala472=
NM_000250.2:c.1391C>A MANE Select	NP_000241.1:p.Pro464His