Canonical Allele Identifier: CA501020742

Gene: MPO

Linked Data

• MyVariant Identifiers: chr17:g.56350221C>T (hg19)

Genomic Alleles

HGVS	Genome Assembly
NC_000017.11:g.58272860C>T , CM000679.2:g.58272860C>T	GRCh38
NC_000017.10:g.56350221C>T , CM000679.1:g.56350221C>T	GRCh37
NC_000017.9:g.53705220C>T	NCBI36
NG_009629.1:g.13076G>A , LRG_84:g.13076G>A

Transcript Alleles

HGVS	Amino-acid Change
ENST00000578493.2:n.1013G>A
ENST00000699291.1:c.805G>A	ENSP00000514272.1:n.805G>A
ENST00000699292.1:n.1215G>A
ENST00000225275.4:c.1680G>A MANE Select	ENSP00000225275.3:p.Gln560=
ENST00000225275.3:c.1680G>A	ENSP00000225275.3:p.Gln560=
ENST00000577220.1:c.138G>A	ENSP00000464668.1:p.Gln46=
NM_000250.1:c.1680G>A , LRG_84t1:c.1680G>A	NP_000241.1:p.Gln560=
XM_011524821.1:c.1866G>A	XP_011523123.1:p.Gln622=
XM_011524822.1:c.1395G>A	XP_011523124.1:p.Gln465=
NM_000250.2:c.1680G>A MANE Select	NP_000241.1:p.Gln560=