Canonical Allele Identifier: CA400370453

Gene: MPO

Linked Data

• MyVariant Identifiers: chr17:g.56350991G>T (hg19) ; chr17:g.58273630G>T (hg38)

Genomic Alleles

HGVS	Genome Assembly
NC_000017.11:g.58273630G>T , CM000679.2:g.58273630G>T	GRCh38
NC_000017.10:g.56350991G>T , CM000679.1:g.56350991G>T	GRCh37
NC_000017.9:g.53705990G>T	NCBI36
NG_009629.1:g.12306C>A , LRG_84:g.12306C>A

Transcript Alleles

HGVS	Amino-acid Change
ENST00000578493.2:n.738C>A
ENST00000699291.1:c.530C>A	ENSP00000514272.1:p.Ala177Asp
ENST00000699292.1:n.445C>A
ENST00000225275.4:c.1405C>A MANE Select	ENSP00000225275.3:p.Pro469Thr
ENST00000225275.3:c.1405C>A	ENSP00000225275.3:p.Pro469Thr
NM_000250.1:c.1405C>A , LRG_84t1:c.1405C>A	NP_000241.1:p.Pro469Thr
XM_011524821.1:c.1591C>A	XP_011523123.1:p.Pro531Thr
XM_011524822.1:c.1120C>A	XP_011523124.1:p.Pro374Thr
XM_011524823.1:c.1430C>A	XP_011523125.1:p.Ala477Asp
NM_000250.2:c.1405C>A MANE Select	NP_000241.1:p.Pro469Thr