Canonical Allele Identifier: CA2638968786

Gene: MPO

Linked Data

• gnomAD v4: 17-58273549-TG-T

Genomic Alleles

HGVS	Genome Assembly
NC_000017.11:g.58273551del , CM000679.2:g.58273551del	GRCh38
NC_000017.10:g.56350912del , CM000679.1:g.56350912del	GRCh37
NC_000017.9:g.53705911del	NCBI36
NG_009629.1:g.12386del , LRG_84:g.12386del

Transcript Alleles

HGVS	Amino-acid Change
ENST00000578493.2:n.818del
ENST00000699291.1:c.610del	ENSP00000514272.1:n.610del
ENST00000699292.1:n.525del
ENST00000225275.4:c.1485del MANE Select	ENSP00000225275.3:p.Asn496MetfsTer?
ENST00000225275.3:c.1485del	ENSP00000225275.3:p.Asn496MetfsTer?
NM_000250.1:c.1485del , LRG_84t1:c.1485del	NP_000241.1:p.Asn496MetfsTer?
XM_011524821.1:c.1671del	XP_011523123.1:p.Asn558MetfsTer?
XM_011524822.1:c.1200del	XP_011523124.1:p.Asn401MetfsTer?
XM_011524823.1:c.*34del	XP_011523125.1:n.*34del
NM_000250.2:c.1485del MANE Select	NP_000241.1:p.Asn496MetfsTer?