Canonical Allele Identifier: CA400370179

Gene: MPO

Linked Data

• MyVariant Identifiers: chr17:g.56350910T>G (hg19) ; chr17:g.58273549T>G (hg38)

Genomic Alleles

HGVS	Genome Assembly
NC_000017.11:g.58273549T>G , CM000679.2:g.58273549T>G	GRCh38
NC_000017.10:g.56350910T>G , CM000679.1:g.56350910T>G	GRCh37
NC_000017.9:g.53705909T>G	NCBI36
NG_009629.1:g.12387A>C , LRG_84:g.12387A>C

Transcript Alleles

HGVS	Amino-acid Change
ENST00000578493.2:n.819A>C
ENST00000699291.1:c.611A>C	ENSP00000514272.1:n.611A>C
ENST00000699292.1:n.526A>C
ENST00000225275.4:c.1486A>C MANE Select	ENSP00000225275.3:p.Asn496His
ENST00000225275.3:c.1486A>C	ENSP00000225275.3:p.Asn496His
NM_000250.1:c.1486A>C , LRG_84t1:c.1486A>C	NP_000241.1:p.Asn496His
XM_011524821.1:c.1672A>C	XP_011523123.1:p.Asn558His
XM_011524822.1:c.1201A>C	XP_011523124.1:p.Asn401His
XM_011524823.1:c.*35A>C	XP_011523125.1:n.*35A>C
NM_000250.2:c.1486A>C MANE Select	NP_000241.1:p.Asn496His