Canonical Allele Identifier: CA2267631360
Gene: MPO HGNC NCBI

Genomic Alleles

HGVS Genome Assembly
NC_000017.11:g.58273657_58273661delinsGGTAA , CM000679.2:g.58273657_58273661delinsGGTAA GRCh38
NC_000017.10:g.56351018_56351022delinsGGTAA , CM000679.1:g.56351018_56351022delinsGGTAA GRCh37
NC_000017.9:g.53706017_53706021delinsGGTAA NCBI36
NG_009629.1:g.12275_12279delinsTTACC , LRG_84:g.12275_12279delinsTTACC

Transcript Alleles

HGVS Amino-acid Change
ENST00000578493.2:n.707_711delinsTTACC
ENST00000699291.1:c.499_503delinsTTACC ENSP00000514272.1:p.Leu167=
ENST00000699292.1:n.414_418delinsTTACC
ENST00000225275.4:c.1374_1378delinsTTACC MANE Select ENSP00000225275.3:p.Thr458=
ENST00000225275.3:c.1374_1378delinsTTACC ENSP00000225275.3:p.Thr458=
NM_000250.1:c.1374_1378delinsTTACC , LRG_84t1:c.1374_1378delinsTTACC NP_000241.1:p.Thr458=
XM_011524821.1:c.1560_1564delinsTTACC XP_011523123.1:p.Thr520=
XM_011524822.1:c.1089_1093delinsTTACC XP_011523124.1:p.Thr363=
XM_011524823.1:c.1399_1403delinsTTACC XP_011523125.1:p.Leu467=
NM_000250.2:c.1374_1378delinsTTACC MANE Select NP_000241.1:p.Thr458=