Canonical Allele Identifier: CA501023655

Gene: MPO

Linked Data

• MyVariant Identifiers: chr17:g.56351016C>A (hg19)

Genomic Alleles

HGVS	Genome Assembly
NC_000017.11:g.58273655C>A , CM000679.2:g.58273655C>A	GRCh38
NC_000017.10:g.56351016C>A , CM000679.1:g.56351016C>A	GRCh37
NC_000017.9:g.53706015C>A	NCBI36
NG_009629.1:g.12281G>T , LRG_84:g.12281G>T

Transcript Alleles

HGVS	Amino-acid Change
ENST00000578493.2:n.713G>T
ENST00000699291.1:c.505G>T	ENSP00000514272.1:p.Gly169Ter
ENST00000699292.1:n.420G>T
ENST00000225275.4:c.1380G>T MANE Select	ENSP00000225275.3:p.Arg460=
ENST00000225275.3:c.1380G>T	ENSP00000225275.3:p.Arg460=
NM_000250.1:c.1380G>T , LRG_84t1:c.1380G>T	NP_000241.1:p.Arg460=
XM_011524821.1:c.1566G>T	XP_011523123.1:p.Arg522=
XM_011524822.1:c.1095G>T	XP_011523124.1:p.Arg365=
XM_011524823.1:c.1405G>T	XP_011523125.1:p.Gly469Ter
NM_000250.2:c.1380G>T MANE Select	NP_000241.1:p.Arg460=