Canonical Allele Identifier: CA501023742

Gene: MPO

Linked Data

• MyVariant Identifiers: chr17:g.56351028G>A (hg19)

Genomic Alleles

HGVS	Genome Assembly
NC_000017.11:g.58273667G>A , CM000679.2:g.58273667G>A	GRCh38
NC_000017.10:g.56351028G>A , CM000679.1:g.56351028G>A	GRCh37
NC_000017.9:g.53706027G>A	NCBI36
NG_009629.1:g.12269C>T , LRG_84:g.12269C>T

Transcript Alleles

HGVS	Amino-acid Change
ENST00000578493.2:n.701C>T
ENST00000699291.1:c.493C>T	ENSP00000514272.1:p.His165Tyr
ENST00000699292.1:n.408C>T
ENST00000225275.4:c.1368C>T MANE Select	ENSP00000225275.3:p.Ile456=
ENST00000225275.3:c.1368C>T	ENSP00000225275.3:p.Ile456=
NM_000250.1:c.1368C>T , LRG_84t1:c.1368C>T	NP_000241.1:p.Ile456=
XM_011524821.1:c.1554C>T	XP_011523123.1:p.Ile518=
XM_011524822.1:c.1083C>T	XP_011523124.1:p.Ile361=
XM_011524823.1:c.1393C>T	XP_011523125.1:p.His465Tyr
NM_000250.2:c.1368C>T MANE Select	NP_000241.1:p.Ile456=