Canonical Allele Identifier: CA2267631389
Gene: MPO HGNC NCBI

Genomic Alleles

HGVS Genome Assembly
NC_000017.11:g.58273705_58273710delinsACTCCT , CM000679.2:g.58273705_58273710delinsACTCCT GRCh38
NC_000017.10:g.56351066_56351071delinsACTCCT , CM000679.1:g.56351066_56351071delinsACTCCT GRCh37
NC_000017.9:g.53706065_53706070delinsACTCCT NCBI36
NG_009629.1:g.12226_12231delinsAGGAGT , LRG_84:g.12226_12231delinsAGGAGT

Transcript Alleles

HGVS Amino-acid Change
ENST00000578493.2:n.699-41_699-36delinsAGGAGT
ENST00000699291.1:c.491-41_491-36delinsAGGAGT ENSP00000514272.1:n.491-41_491-36delinsAGGAGT
ENST00000699292.1:n.365_370delinsAGGAGT
ENST00000225275.4:c.1366-41_1366-36delinsAGGAGT MANE Select ENSP00000225275.3:n.1366-41_1366-36delinsAGGAGT
ENST00000225275.3:c.1366-41_1366-36delinsAGGAGT ENSP00000225275.3:n.1366-41_1366-36delinsAGGAGT
NM_000250.1:c.1366-41_1366-36delinsAGGAGT , LRG_84t1:c.1366-41_1366-36delinsAGGAGT NP_000241.1:n.1366-41_1366-36delinsAGGAGT
XM_011524821.1:c.1552-41_1552-36delinsAGGAGT XP_011523123.1:n.1552-41_1552-36delinsAGGAGT
XM_011524822.1:c.1081-41_1081-36delinsAGGAGT XP_011523124.1:n.1081-41_1081-36delinsAGGAGT
XM_011524823.1:c.1391-41_1391-36delinsAGGAGT XP_011523125.1:n.1391-41_1391-36delinsAGGAGT
NM_000250.2:c.1366-41_1366-36delinsAGGAGT MANE Select NP_000241.1:n.1366-41_1366-36delinsAGGAGT