Canonical Allele Identifier: CA400370366

Gene: MPO

Linked Data

• MyVariant Identifiers: chr17:g.56350967G>T (hg19) ; chr17:g.58273606G>T (hg38)

Genomic Alleles

HGVS	Genome Assembly
NC_000017.11:g.58273606G>T , CM000679.2:g.58273606G>T	GRCh38
NC_000017.10:g.56350967G>T , CM000679.1:g.56350967G>T	GRCh37
NC_000017.9:g.53705966G>T	NCBI36
NG_009629.1:g.12330C>A , LRG_84:g.12330C>A

Transcript Alleles

HGVS	Amino-acid Change
ENST00000578493.2:n.762C>A
ENST00000699291.1:c.554C>A	ENSP00000514272.1:p.Ala185Asp
ENST00000699292.1:n.469C>A
ENST00000225275.4:c.1429C>A MANE Select	ENSP00000225275.3:p.Pro477Thr
ENST00000225275.3:c.1429C>A	ENSP00000225275.3:p.Pro477Thr
NM_000250.1:c.1429C>A , LRG_84t1:c.1429C>A	NP_000241.1:p.Pro477Thr
XM_011524821.1:c.1615C>A	XP_011523123.1:p.Pro539Thr
XM_011524822.1:c.1144C>A	XP_011523124.1:p.Pro382Thr
XM_011524823.1:c.1454C>A	XP_011523125.1:p.Ala485Asp
NM_000250.2:c.1429C>A MANE Select	NP_000241.1:p.Pro477Thr