Canonical Allele Identifier: CA400370293

Gene: MPO

Linked Data

• MyVariant Identifiers: chr17:g.56350946C>A (hg19) ; chr17:g.58273585C>A (hg38)

Genomic Alleles

HGVS	Genome Assembly
NC_000017.11:g.58273585C>A , CM000679.2:g.58273585C>A	GRCh38
NC_000017.10:g.56350946C>A , CM000679.1:g.56350946C>A	GRCh37
NC_000017.9:g.53705945C>A	NCBI36
NG_009629.1:g.12351G>T , LRG_84:g.12351G>T

Transcript Alleles

HGVS	Amino-acid Change
ENST00000578493.2:n.783G>T
ENST00000699291.1:c.575G>T	ENSP00000514272.1:p.Ter192Leu
ENST00000699292.1:n.490G>T
ENST00000225275.4:c.1450G>T MANE Select	ENSP00000225275.3:p.Asp484Tyr
ENST00000225275.3:c.1450G>T	ENSP00000225275.3:p.Asp484Tyr
NM_000250.1:c.1450G>T , LRG_84t1:c.1450G>T	NP_000241.1:p.Asp484Tyr
XM_011524821.1:c.1636G>T	XP_011523123.1:p.Asp546Tyr
XM_011524822.1:c.1165G>T	XP_011523124.1:p.Asp389Tyr
XM_011524823.1:c.1475G>T	XP_011523125.1:p.Ter492Leu
NM_000250.2:c.1450G>T MANE Select	NP_000241.1:p.Asp484Tyr