Canonical Allele Identifier: CA400370556

Gene: MPO

Linked Data

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

Genomic Alleles

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

Transcript Alleles

HGVS	Amino-acid Change
ENST00000578493.2:n.703T>C
ENST00000699291.1:c.495T>C	ENSP00000514272.1:p.His165=
ENST00000699292.1:n.410T>C
ENST00000225275.4:c.1370T>C MANE Select	ENSP00000225275.3:p.Ile457Thr
ENST00000225275.3:c.1370T>C	ENSP00000225275.3:p.Ile457Thr
NM_000250.1:c.1370T>C , LRG_84t1:c.1370T>C	NP_000241.1:p.Ile457Thr
XM_011524821.1:c.1556T>C	XP_011523123.1:p.Ile519Thr
XM_011524822.1:c.1085T>C	XP_011523124.1:p.Ile362Thr
XM_011524823.1:c.1395T>C	XP_011523125.1:p.His465=
NM_000250.2:c.1370T>C MANE Select	NP_000241.1:p.Ile457Thr