Canonical Allele Identifier: CA501023162

Gene: MPO

Linked Data

• MyVariant Identifiers: chr17:g.56350979T>G (hg19)

Genomic Alleles

HGVS	Genome Assembly
NC_000017.11:g.58273618T>G , CM000679.2:g.58273618T>G	GRCh38
NC_000017.10:g.56350979T>G , CM000679.1:g.56350979T>G	GRCh37
NC_000017.9:g.53705978T>G	NCBI36
NG_009629.1:g.12318A>C , LRG_84:g.12318A>C

Transcript Alleles

HGVS	Amino-acid Change
ENST00000578493.2:n.750A>C
ENST00000699291.1:c.542A>C	ENSP00000514272.1:p.Glu181Ala
ENST00000699292.1:n.457A>C
ENST00000225275.4:c.1417A>C MANE Select	ENSP00000225275.3:p.Arg473=
ENST00000225275.3:c.1417A>C	ENSP00000225275.3:p.Arg473=
NM_000250.1:c.1417A>C , LRG_84t1:c.1417A>C	NP_000241.1:p.Arg473=
XM_011524821.1:c.1603A>C	XP_011523123.1:p.Arg535=
XM_011524822.1:c.1132A>C	XP_011523124.1:p.Arg378=
XM_011524823.1:c.1442A>C	XP_011523125.1:p.Glu481Ala
NM_000250.2:c.1417A>C MANE Select	NP_000241.1:p.Arg473=