Canonical Allele Identifier: CA8670623
Gene: MPO HGNC NCBI

Linked Data

dbSNP Id: rs558838925

Genomic Alleles

HGVS Genome Assembly
NC_000017.11:g.58273558C>T , CM000679.2:g.58273558C>T GRCh38
NC_000017.10:g.56350919C>T , CM000679.1:g.56350919C>T GRCh37
NC_000017.9:g.53705918C>T NCBI36
NG_009629.1:g.12378G>A , LRG_84:g.12378G>A

Transcript Alleles

HGVS Amino-acid Change
ENST00000578493.2:n.810G>A
ENST00000699291.1:c.602G>A ENSP00000514272.1:n.602G>A
ENST00000699292.1:n.517G>A
ENST00000225275.4:c.1477G>A MANE Select ENSP00000225275.3:p.Val493Ile
ENST00000225275.3:c.1477G>A ENSP00000225275.3:p.Val493Ile
NM_000250.1:c.1477G>A , LRG_84t1:c.1477G>A NP_000241.1:p.Val493Ile
XM_011524821.1:c.1663G>A XP_011523123.1:p.Val555Ile
XM_011524822.1:c.1192G>A XP_011523124.1:p.Val398Ile
XM_011524823.1:c.*26G>A XP_011523125.1:n.*26G>A
NM_000250.2:c.1477G>A MANE Select NP_000241.1:p.Val493Ile