Canonical Allele Identifier: CA2267631387

Gene: MPO

Genomic Alleles

HGVS	Genome Assembly
NC_000017.11:g.58273701_58273703delinsACC , CM000679.2:g.58273701_58273703delinsACC	GRCh38
NC_000017.10:g.56351062_56351064delinsACC , CM000679.1:g.56351062_56351064delinsACC	GRCh37
NC_000017.9:g.53706061_53706063delinsACC	NCBI36
NG_009629.1:g.12233_12235delinsGGT , LRG_84:g.12233_12235delinsGGT

Transcript Alleles

HGVS	Amino-acid Change
ENST00000578493.2:n.699-34_699-32delinsGGT
ENST00000699291.1:c.491-34_491-32delinsGGT	ENSP00000514272.1:n.491-34_491-32delinsGGT
ENST00000699292.1:n.372_374delinsGGT
ENST00000225275.4:c.1366-34_1366-32delinsGGT MANE Select	ENSP00000225275.3:n.1366-34_1366-32delinsGGT
ENST00000225275.3:c.1366-34_1366-32delinsGGT	ENSP00000225275.3:n.1366-34_1366-32delinsGGT
NM_000250.1:c.1366-34_1366-32delinsGGT , LRG_84t1:c.1366-34_1366-32delinsGGT	NP_000241.1:n.1366-34_1366-32delinsGGT
XM_011524821.1:c.1552-34_1552-32delinsGGT	XP_011523123.1:n.1552-34_1552-32delinsGGT
XM_011524822.1:c.1081-34_1081-32delinsGGT	XP_011523124.1:n.1081-34_1081-32delinsGGT
XM_011524823.1:c.1391-34_1391-32delinsGGT	XP_011523125.1:n.1391-34_1391-32delinsGGT
NM_000250.2:c.1366-34_1366-32delinsGGT MANE Select	NP_000241.1:n.1366-34_1366-32delinsGGT