Canonical Allele Identifier: CA2267631197
Gene: MPO HGNC NCBI

Genomic Alleles

HGVS Genome Assembly
NC_000017.11:g.58273319C= , CM000679.2:g.58273319C= GRCh38
NC_000017.10:g.56350680C= , CM000679.1:g.56350680C= GRCh37
NC_000017.9:g.53705679C= NCBI36
NG_009629.1:g.12617G= , LRG_84:g.12617G=

Transcript Alleles

HGVS Amino-acid Change
ENST00000578493.2:n.954+95G=
ENST00000699291.1:c.746+95G= ENSP00000514272.1:n.746+95G=
ENST00000699292.1:n.756G=
ENST00000225275.4:c.1621+95G= MANE Select ENSP00000225275.3:n.1621+95G=
ENST00000225275.3:c.1621+95G= ENSP00000225275.3:n.1621+95G=
ENST00000577220.1:c.79+95G= ENSP00000464668.1:n.79+95G=
NM_000250.1:c.1621+95G= , LRG_84t1:c.1621+95G= NP_000241.1:n.1621+95G=
XM_011524821.1:c.1807+95G= XP_011523123.1:n.1807+95G=
XM_011524822.1:c.1336+95G= XP_011523124.1:n.1336+95G=
NM_000250.2:c.1621+95G= MANE Select NP_000241.1:n.1621+95G=