Canonical Allele Identifier: CA501023557

Gene: MPO

Linked Data

• MyVariant Identifiers: chr17:g.56350998C>T (hg19)

Genomic Alleles

HGVS	Genome Assembly
NC_000017.11:g.58273637C>T , CM000679.2:g.58273637C>T	GRCh38
NC_000017.10:g.56350998C>T , CM000679.1:g.56350998C>T	GRCh37
NC_000017.9:g.53705997C>T	NCBI36
NG_009629.1:g.12299G>A , LRG_84:g.12299G>A

Transcript Alleles

HGVS	Amino-acid Change
ENST00000578493.2:n.731G>A
ENST00000699291.1:c.523G>A	ENSP00000514272.1:p.Ala175Thr
ENST00000699292.1:n.438G>A
ENST00000225275.4:c.1398G>A MANE Select	ENSP00000225275.3:p.Val466=
ENST00000225275.3:c.1398G>A	ENSP00000225275.3:p.Val466=
NM_000250.1:c.1398G>A , LRG_84t1:c.1398G>A	NP_000241.1:p.Val466=
XM_011524821.1:c.1584G>A	XP_011523123.1:p.Val528=
XM_011524822.1:c.1113G>A	XP_011523124.1:p.Val371=
XM_011524823.1:c.1423G>A	XP_011523125.1:p.Ala475Thr
NM_000250.2:c.1398G>A MANE Select	NP_000241.1:p.Val466=