Canonical Allele Identifier: CA400370143
Gene: MPO HGNC NCBI

Linked Data

Genomic Alleles

HGVS Genome Assembly
NC_000017.11:g.58273540G>T , CM000679.2:g.58273540G>T GRCh38
NC_000017.10:g.56350901G>T , CM000679.1:g.56350901G>T GRCh37
NC_000017.9:g.53705900G>T NCBI36
NG_009629.1:g.12396C>A , LRG_84:g.12396C>A

Transcript Alleles

HGVS Amino-acid Change
ENST00000578493.2:n.828C>A
ENST00000699291.1:c.620C>A ENSP00000514272.1:n.620C>A
ENST00000699292.1:n.535C>A
ENST00000225275.4:c.1495C>A MANE Select ENSP00000225275.3:p.Arg499Ser
ENST00000225275.3:c.1495C>A ENSP00000225275.3:p.Arg499Ser
NM_000250.1:c.1495C>A , LRG_84t1:c.1495C>A NP_000241.1:p.Arg499Ser
XM_011524821.1:c.1681C>A XP_011523123.1:p.Arg561Ser
XM_011524822.1:c.1210C>A XP_011523124.1:p.Arg404Ser
XM_011524823.1:c.*44C>A XP_011523125.1:n.*44C>A
NM_000250.2:c.1495C>A MANE Select NP_000241.1:p.Arg499Ser