Canonical Allele Identifier: CA2267630074
Gene: MPO HGNC NCBI

Genomic Alleles

HGVS Genome Assembly
NC_000017.11:g.58270865T= , CM000679.2:g.58270865T= GRCh38
NC_000017.10:g.56348226T= , CM000679.1:g.56348226T= GRCh37
NC_000017.9:g.53703225T= NCBI36
NG_009629.1:g.15071A= , LRG_84:g.15071A=

Transcript Alleles

HGVS Amino-acid Change
NM_000250.2:c.2031-2A= MANE Select NP_000241.1:n.2031-2A=
ENST00000225275.4:c.2031-2A= MANE Select ENSP00000225275.3:n.2031-2A=
NM_000250.1:c.2031-2A= , LRG_84t1:c.2031-2A= NP_000241.1:n.2031-2A=
ENST00000225275.3:c.2031-2A= ENSP00000225275.3:n.2031-2A=
ENST00000577220.1:c.184-60A= ENSP00000464668.1:n.184-60A=
ENST00000578493.2:n.1364-2A=
ENST00000699291.1:c.1156-2A= ENSP00000514272.1:n.1156-2A=
ENST00000699292.1:n.1566-2A=
XM_011524821.1:c.2217-2A= XP_011523123.1:n.2217-2A=
XM_011524822.1:c.1746-2A= XP_011523124.1:n.1746-2A=