Canonical Allele Identifier: CA2638968896

Gene: MPO

Linked Data

• gnomAD v4: 17-58273569-CGT-C

Genomic Alleles

HGVS	Genome Assembly
NC_000017.11:g.58273571_58273572del , CM000679.2:g.58273571_58273572del	GRCh38
NC_000017.10:g.56350932_56350933del , CM000679.1:g.56350932_56350933del	GRCh37
NC_000017.9:g.53705931_53705932del	NCBI36
NG_009629.1:g.12365_12366del , LRG_84:g.12365_12366del

Transcript Alleles

HGVS	Amino-acid Change
ENST00000578493.2:n.797_798del
ENST00000699291.1:c.589_590del	ENSP00000514272.1:n.589_590del
ENST00000699292.1:n.504_505del
ENST00000225275.4:c.1464_1465del MANE Select	ENSP00000225275.3:p.Arg489HisfsTer?
ENST00000225275.3:c.1464_1465del	ENSP00000225275.3:p.Arg489HisfsTer?
NM_000250.1:c.1464_1465del , LRG_84t1:c.1464_1465del	NP_000241.1:p.Arg489HisfsTer?
XM_011524821.1:c.1650_1651del	XP_011523123.1:p.Arg551HisfsTer?
XM_011524822.1:c.1179_1180del	XP_011523124.1:p.Arg394HisfsTer?
XM_011524823.1:c.*13_*14del	XP_011523125.1:n.*13_*14del
NM_000250.2:c.1464_1465del MANE Select	NP_000241.1:p.Arg489HisfsTer?