Canonical Allele Identifier: CA2267631221
Gene: MPO HGNC NCBI

Genomic Alleles

HGVS Genome Assembly
NC_000017.11:g.58273372T= , CM000679.2:g.58273372T= GRCh38
NC_000017.10:g.56350733T= , CM000679.1:g.56350733T= GRCh37
NC_000017.9:g.53705732T= NCBI36
NG_009629.1:g.12564A= , LRG_84:g.12564A=

Transcript Alleles

HGVS Amino-acid change
ENST00000578493.2:n.954+42A=
ENST00000699291.1:c.746+42A= ENSP00000514272.1:n.746+42A=
ENST00000699292.1:n.703A=
ENST00000225275.4:c.1621+42A= MANE Select ENSP00000225275.3:n.1621+42A=
ENST00000225275.3:c.1621+42A= ENSP00000225275.3:n.1621+42A=
ENST00000577220.1:c.79+42A= ENSP00000464668.1:n.79+42A=
NM_000250.1:c.1621+42A= , LRG_84t1:c.1621+42A= NP_000241.1:n.1621+42A=
XM_011524821.1:c.1807+42A= XP_011523123.1:n.1807+42A=
XM_011524822.1:c.1336+42A= XP_011523124.1:n.1336+42A=
NM_000250.2:c.1621+42A= MANE Select NP_000241.1:n.1621+42A=