Canonical Allele Identifier: CA2267634662
Gene: MPO HGNC NCBI

Genomic Alleles

HGVS Genome Assembly
NC_000017.11:g.58280520G= , CM000679.2:g.58280520G= GRCh38
NC_000017.10:g.56357881G= , CM000679.1:g.56357881G= GRCh37
NC_000017.9:g.53712880G= NCBI36
NG_009629.1:g.5416C= , LRG_84:g.5416C=

Transcript Alleles

HGVS Amino-acid change
ENST00000225275.4:c.155-61C= MANE Select ENSP00000225275.3:n.155-61C=
ENST00000225275.3:c.155-61C= ENSP00000225275.3:n.155-61C=
ENST00000580005.1:n.84-61C=
NM_000250.1:c.155-61C= , LRG_84t1:c.155-61C= NP_000241.1:n.155-61C=
XM_011524821.1:c.341-61C= XP_011523123.1:n.341-61C=
XM_011524822.1:c.-38+85C= XP_011523124.1:n.-38+85C=
XM_011524823.1:c.341-61C= XP_011523125.1:n.341-61C=
NM_000250.2:c.155-61C= MANE Select NP_000241.1:n.155-61C=