Canonical Allele Identifier: CA2267634583
Gene: MPO HGNC NCBI

Genomic Alleles

HGVS Genome Assembly
NC_000017.11:g.58280361C= , CM000679.2:g.58280361C= GRCh38
NC_000017.10:g.56357722C= , CM000679.1:g.56357722C= GRCh37
NC_000017.9:g.53712721C= NCBI36
NG_009629.1:g.5575G= , LRG_84:g.5575G=

Transcript Alleles

HGVS Amino-acid change
ENST00000225275.4:c.248+5G= MANE Select ENSP00000225275.3:n.248+5G=
ENST00000225275.3:c.248+5G= ENSP00000225275.3:n.248+5G=
ENST00000580005.1:n.182G=
NM_000250.1:c.248+5G= , LRG_84t1:c.248+5G= NP_000241.1:n.248+5G=
XM_011524821.1:c.434+5G= XP_011523123.1:n.434+5G=
XM_011524822.1:c.-38+244G= XP_011523124.1:n.-38+244G=
XM_011524823.1:c.434+5G= XP_011523125.1:n.434+5G=
NM_000250.2:c.248+5G= MANE Select NP_000241.1:n.248+5G=