Canonical Allele Identifier: CA400370149

Gene: MPO

Linked Data

• MyVariant Identifiers: chr17:g.56350903A>T (hg19) ; chr17:g.58273542A>T (hg38)

Genomic Alleles

HGVS	Genome Assembly
NC_000017.11:g.58273542A>T , CM000679.2:g.58273542A>T	GRCh38
NC_000017.10:g.56350903A>T , CM000679.1:g.56350903A>T	GRCh37
NC_000017.9:g.53705902A>T	NCBI36
NG_009629.1:g.12394T>A , LRG_84:g.12394T>A

Transcript Alleles

HGVS	Amino-acid Change
ENST00000578493.2:n.826T>A
ENST00000699291.1:c.618T>A	ENSP00000514272.1:n.618T>A
ENST00000699292.1:n.533T>A
ENST00000225275.4:c.1493T>A MANE Select	ENSP00000225275.3:p.Phe498Tyr
ENST00000225275.3:c.1493T>A	ENSP00000225275.3:p.Phe498Tyr
NM_000250.1:c.1493T>A , LRG_84t1:c.1493T>A	NP_000241.1:p.Phe498Tyr
XM_011524821.1:c.1679T>A	XP_011523123.1:p.Phe560Tyr
XM_011524822.1:c.1208T>A	XP_011523124.1:p.Phe403Tyr
XM_011524823.1:c.*42T>A	XP_011523125.1:n.*42T>A
NM_000250.2:c.1493T>A MANE Select	NP_000241.1:p.Phe498Tyr