Canonical Allele Identifier: CA400370193

Gene: MPO

Linked Data

• MyVariant Identifiers: chr17:g.56350915A>T (hg19) ; chr17:g.58273554A>T (hg38)

Genomic Alleles

HGVS	Genome Assembly
NC_000017.11:g.58273554A>T , CM000679.2:g.58273554A>T	GRCh38
NC_000017.10:g.56350915A>T , CM000679.1:g.56350915A>T	GRCh37
NC_000017.9:g.53705914A>T	NCBI36
NG_009629.1:g.12382T>A , LRG_84:g.12382T>A

Transcript Alleles

HGVS	Amino-acid Change
ENST00000578493.2:n.814T>A
ENST00000699291.1:c.606T>A	ENSP00000514272.1:n.606T>A
ENST00000699292.1:n.521T>A
ENST00000225275.4:c.1481T>A MANE Select	ENSP00000225275.3:p.Phe494Tyr
ENST00000225275.3:c.1481T>A	ENSP00000225275.3:p.Phe494Tyr
NM_000250.1:c.1481T>A , LRG_84t1:c.1481T>A	NP_000241.1:p.Phe494Tyr
XM_011524821.1:c.1667T>A	XP_011523123.1:p.Phe556Tyr
XM_011524822.1:c.1196T>A	XP_011523124.1:p.Phe399Tyr
XM_011524823.1:c.*30T>A	XP_011523125.1:n.*30T>A
NM_000250.2:c.1481T>A MANE Select	NP_000241.1:p.Phe494Tyr