Canonical Allele Identifier: CA2267631236
Gene: MPO HGNC NCBI

Genomic Alleles

HGVS Genome Assembly
NC_000017.11:g.58273412A= , CM000679.2:g.58273412A= GRCh38
NC_000017.10:g.56350773A= , CM000679.1:g.56350773A= GRCh37
NC_000017.9:g.53705772A= NCBI36
NG_009629.1:g.12524T= , LRG_84:g.12524T=

Transcript Alleles

HGVS Amino-acid change
ENST00000578493.2:n.954+2T=
ENST00000699291.1:c.746+2T= ENSP00000514272.1:n.746+2T=
ENST00000699292.1:n.663T=
ENST00000225275.4:c.1621+2T= MANE Select ENSP00000225275.3:n.1621+2T=
ENST00000225275.3:c.1621+2T= ENSP00000225275.3:n.1621+2T=
ENST00000577220.1:c.79+2T= ENSP00000464668.1:n.79+2T=
NM_000250.1:c.1621+2T= , LRG_84t1:c.1621+2T= NP_000241.1:n.1621+2T=
XM_011524821.1:c.1807+2T= XP_011523123.1:n.1807+2T=
XM_011524822.1:c.1336+2T= XP_011523124.1:n.1336+2T=
NM_000250.2:c.1621+2T= MANE Select NP_000241.1:n.1621+2T=