Canonical Allele Identifier: CA400368969
Gene: MPO HGNC NCBI

Linked Data

Genomic Alleles

HGVS Genome Assembly
NC_000017.11:g.58272753A>C , CM000679.2:g.58272753A>C GRCh38
NC_000017.10:g.56350114A>C , CM000679.1:g.56350114A>C GRCh37
NC_000017.9:g.53705113A>C NCBI36
NG_009629.1:g.13183T>G , LRG_84:g.13183T>G

Transcript Alleles

HGVS Amino-acid change
ENST00000578493.2:n.1120T>G
ENST00000699291.1:c.912T>G ENSP00000514272.1:n.912T>G
ENST00000699292.1:n.1322T>G
ENST00000225275.4:c.1787T>G MANE Select ENSP00000225275.3:p.Leu596Arg
ENST00000225275.3:c.1787T>G ENSP00000225275.3:p.Leu596Arg
ENST00000577220.1:c.183+62T>G ENSP00000464668.1:n.183+62T>G
NM_000250.1:c.1787T>G , LRG_84t1:c.1787T>G NP_000241.1:p.Leu596Arg
XM_011524821.1:c.1973T>G XP_011523123.1:p.Leu658Arg
XM_011524822.1:c.1502T>G XP_011523124.1:p.Leu501Arg
NM_000250.2:c.1787T>G MANE Select NP_000241.1:p.Leu596Arg