Canonical Allele Identifier: CA2638968766

Gene: MPO

Linked Data

• gnomAD v4: 17-58273545-GCATTGGTGAAGA-G

Genomic Alleles

HGVS	Genome Assembly
NC_000017.11:g.58273547_58273558del , CM000679.2:g.58273547_58273558del	GRCh38
NC_000017.10:g.56350908_56350919del , CM000679.1:g.56350908_56350919del	GRCh37
NC_000017.9:g.53705907_53705918del	NCBI36
NG_009629.1:g.12379_12390del , LRG_84:g.12379_12390del

Transcript Alleles

HGVS	Amino-acid Change
ENST00000578493.2:n.811_822del
ENST00000699291.1:c.603_614del	ENSP00000514272.1:n.603_614del
ENST00000699292.1:n.518_529del
ENST00000225275.4:c.1478_1489del MANE Select	ENSP00000225275.3:p.Val493_Asn496del
ENST00000225275.3:c.1478_1489del	ENSP00000225275.3:p.Val493_Asn496del
NM_000250.1:c.1478_1489del , LRG_84t1:c.1478_1489del	NP_000241.1:p.Val493_Asn496del
XM_011524821.1:c.1664_1675del	XP_011523123.1:p.Val555_Asn558del
XM_011524822.1:c.1193_1204del	XP_011523124.1:p.Val398_Asn401del
XM_011524823.1:c.*27_*38del	XP_011523125.1:n.*27_*38del
NM_000250.2:c.1478_1489del MANE Select	NP_000241.1:p.Val493_Asn496del