Canonical Allele Identifier: CA501020198
Gene: MPO HGNC NCBI

Linked Data

MyVariant Identifiers: chr17:g.56350116G>T (hg19)

Genomic Alleles

HGVS Genome Assembly
NC_000017.11:g.58272755G>T , CM000679.2:g.58272755G>T GRCh38
NC_000017.10:g.56350116G>T , CM000679.1:g.56350116G>T GRCh37
NC_000017.9:g.53705115G>T NCBI36
NG_009629.1:g.13181C>A , LRG_84:g.13181C>A

Transcript Alleles

HGVS Amino-acid change
ENST00000578493.2:n.1118C>A
ENST00000699291.1:c.910C>A ENSP00000514272.1:n.910C>A
ENST00000699292.1:n.1320C>A
ENST00000225275.4:c.1785C>A MANE Select ENSP00000225275.3:p.Gly595=
ENST00000225275.3:c.1785C>A ENSP00000225275.3:p.Gly595=
ENST00000577220.1:c.183+60C>A ENSP00000464668.1:n.183+60C>A
NM_000250.1:c.1785C>A , LRG_84t1:c.1785C>A NP_000241.1:p.Gly595=
XM_011524821.1:c.1971C>A XP_011523123.1:p.Gly657=
XM_011524822.1:c.1500C>A XP_011523124.1:p.Gly500=
NM_000250.2:c.1785C>A MANE Select NP_000241.1:p.Gly595=