Canonical Allele Identifier: CA2267631313
Gene: MPO HGNC NCBI

Genomic Alleles

HGVS Genome Assembly
NC_000017.11:g.58273556G= , CM000679.2:g.58273556G= GRCh38
NC_000017.10:g.56350917G= , CM000679.1:g.56350917G= GRCh37
NC_000017.9:g.53705916G= NCBI36
NG_009629.1:g.12380C= , LRG_84:g.12380C=

Transcript Alleles

HGVS Amino-acid Change
ENST00000578493.2:n.812C=
ENST00000699291.1:c.604C= ENSP00000514272.1:n.604C=
ENST00000699292.1:n.519C=
ENST00000225275.4:c.1479C= MANE Select ENSP00000225275.3:p.Val493=
ENST00000225275.3:c.1479C= ENSP00000225275.3:p.Val493=
NM_000250.1:c.1479C= , LRG_84t1:c.1479C= NP_000241.1:p.Val493=
XM_011524821.1:c.1665C= XP_011523123.1:p.Val555=
XM_011524822.1:c.1194C= XP_011523124.1:p.Val398=
XM_011524823.1:c.*28C= XP_011523125.1:n.*28C=
NM_000250.2:c.1479C= MANE Select NP_000241.1:p.Val493=