Canonical Allele Identifier: CA501020728

Gene: MPO

Linked Data

• MyVariant Identifiers: chr17:g.56350218G>A (hg19)

Genomic Alleles

HGVS	Genome Assembly
NC_000017.11:g.58272857G>A , CM000679.2:g.58272857G>A	GRCh38
NC_000017.10:g.56350218G>A , CM000679.1:g.56350218G>A	GRCh37
NC_000017.9:g.53705217G>A	NCBI36
NG_009629.1:g.13079C>T , LRG_84:g.13079C>T

Transcript Alleles

HGVS	Amino-acid Change
ENST00000578493.2:n.1016C>T
ENST00000699291.1:c.808C>T	ENSP00000514272.1:n.808C>T
ENST00000699292.1:n.1218C>T
ENST00000225275.4:c.1683C>T MANE Select	ENSP00000225275.3:p.Asn561=
ENST00000225275.3:c.1683C>T	ENSP00000225275.3:p.Asn561=
ENST00000577220.1:c.141C>T	ENSP00000464668.1:p.Asn47=
NM_000250.1:c.1683C>T , LRG_84t1:c.1683C>T	NP_000241.1:p.Asn561=
XM_011524821.1:c.1869C>T	XP_011523123.1:p.Asn623=
XM_011524822.1:c.1398C>T	XP_011523124.1:p.Asn466=
NM_000250.2:c.1683C>T MANE Select	NP_000241.1:p.Asn561=