Canonical Allele Identifier: CA2809973211
Gene: MPO HGNC NCBI

Genomic Alleles

HGVS Genome Assembly
NC_000017.11:g.58272744T>C , CM000679.2:g.58272744T>C GRCh38
NC_000017.10:g.56350105T>C , CM000679.1:g.56350105T>C GRCh37
NC_000017.9:g.53705104T>C NCBI36
NG_009629.1:g.13192A>G , LRG_84:g.13192A>G

Transcript Alleles

HGVS Amino-acid Change
ENST00000578493.2:n.1125+4A>G
ENST00000699291.1:c.917+4A>G ENSP00000514272.1:n.917+4A>G
ENST00000699292.1:n.1327+4A>G
ENST00000225275.4:c.1792+4A>G MANE Select ENSP00000225275.3:n.1792+4A>G
ENST00000225275.3:c.1792+4A>G ENSP00000225275.3:n.1792+4A>G
ENST00000577220.1:c.183+71A>G ENSP00000464668.1:n.183+71A>G
NM_000250.1:c.1792+4A>G , LRG_84t1:c.1792+4A>G NP_000241.1:n.1792+4A>G
XM_011524821.1:c.1978+4A>G XP_011523123.1:n.1978+4A>G
XM_011524822.1:c.1507+4A>G XP_011523124.1:n.1507+4A>G
NM_000250.2:c.1792+4A>G MANE Select NP_000241.1:n.1792+4A>G