Canonical Allele Identifier: CA645590792
Gene: MPO HGNC NCBI

Linked Data

Genomic Alleles

HGVS Genome Assembly
NC_000017.11:g.58280372_58280373insT , CM000679.2:g.58280372_58280373insT GRCh38
NC_000017.10:g.56357733_56357734insT , CM000679.1:g.56357733_56357734insT GRCh37
NC_000017.9:g.53712732_53712733insT NCBI36
NG_009629.1:g.5563_5564insA , LRG_84:g.5563_5564insA

Transcript Alleles

HGVS Amino-acid change
ENST00000225275.4:c.241_242insA MANE Select ENSP00000225275.3:p.Arg81GlnfsTer?
ENST00000225275.3:c.241_242insA ENSP00000225275.3:p.Arg81GlnfsTer?
ENST00000580005.1:n.170_171insA
NM_000250.1:c.241_242insA , LRG_84t1:c.241_242insA NP_000241.1:p.Arg81GlnfsTer?
XM_011524821.1:c.427_428insA XP_011523123.1:p.Arg143GlnfsTer?
XM_011524822.1:c.-38+232_-38+233insA XP_011523124.1:n.-38+232_-38+233insA
XM_011524823.1:c.427_428insA XP_011523125.1:p.Arg143GlnfsTer?
NM_000250.2:c.241_242insA MANE Select NP_000241.1:p.Arg81GlnfsTer?