Canonical Allele Identifier: CA400370557

Gene: MPO

Linked Data

• MyVariant Identifiers: chr17:g.56351026A>T (hg19) ; chr17:g.58273665A>T (hg38)

Genomic Alleles

HGVS	Genome Assembly
NC_000017.11:g.58273665A>T , CM000679.2:g.58273665A>T	GRCh38
NC_000017.10:g.56351026A>T , CM000679.1:g.56351026A>T	GRCh37
NC_000017.9:g.53706025A>T	NCBI36
NG_009629.1:g.12271T>A , LRG_84:g.12271T>A

Transcript Alleles

HGVS	Amino-acid Change
ENST00000578493.2:n.703T>A
ENST00000699291.1:c.495T>A	ENSP00000514272.1:p.His165Gln
ENST00000699292.1:n.410T>A
ENST00000225275.4:c.1370T>A MANE Select	ENSP00000225275.3:p.Ile457Asn
ENST00000225275.3:c.1370T>A	ENSP00000225275.3:p.Ile457Asn
NM_000250.1:c.1370T>A , LRG_84t1:c.1370T>A	NP_000241.1:p.Ile457Asn
XM_011524821.1:c.1556T>A	XP_011523123.1:p.Ile519Asn
XM_011524822.1:c.1085T>A	XP_011523124.1:p.Ile362Asn
XM_011524823.1:c.1395T>A	XP_011523125.1:p.His465Gln
NM_000250.2:c.1370T>A MANE Select	NP_000241.1:p.Ile457Asn