Canonical Allele Identifier: CA400370402

Gene: MPO

Linked Data

• MyVariant Identifiers: chr17:g.56350977C>A (hg19) ; chr17:g.58273616C>A (hg38)

Genomic Alleles

HGVS	Genome Assembly
NC_000017.11:g.58273616C>A , CM000679.2:g.58273616C>A	GRCh38
NC_000017.10:g.56350977C>A , CM000679.1:g.56350977C>A	GRCh37
NC_000017.9:g.53705976C>A	NCBI36
NG_009629.1:g.12320G>T , LRG_84:g.12320G>T

Transcript Alleles

HGVS	Amino-acid Change
ENST00000578493.2:n.752G>T
ENST00000699291.1:c.544G>T	ENSP00000514272.1:p.Glu182Ter
ENST00000699292.1:n.459G>T
ENST00000225275.4:c.1419G>T MANE Select	ENSP00000225275.3:p.Arg473Ser
ENST00000225275.3:c.1419G>T	ENSP00000225275.3:p.Arg473Ser
NM_000250.1:c.1419G>T , LRG_84t1:c.1419G>T	NP_000241.1:p.Arg473Ser
XM_011524821.1:c.1605G>T	XP_011523123.1:p.Arg535Ser
XM_011524822.1:c.1134G>T	XP_011523124.1:p.Arg378Ser
XM_011524823.1:c.1444G>T	XP_011523125.1:p.Glu482Ter
NM_000250.2:c.1419G>T MANE Select	NP_000241.1:p.Arg473Ser