Canonical Allele Identifier: CA2638968861

Gene: MPO

Linked Data

• gnomAD v4: 17-58273564-C-CGATGCG

Genomic Alleles

HGVS	Genome Assembly
NC_000017.11:g.58273565_58273570dup , CM000679.2:g.58273565_58273570dup	GRCh38
NC_000017.10:g.56350926_56350931dup , CM000679.1:g.56350926_56350931dup	GRCh37
NC_000017.9:g.53705925_53705930dup	NCBI36
NG_009629.1:g.12366_12371dup , LRG_84:g.12366_12371dup

Transcript Alleles

HGVS	Amino-acid Change
ENST00000578493.2:n.798_803dup
ENST00000699291.1:c.590_595dup	ENSP00000514272.1:n.590_595dup
ENST00000699292.1:n.505_510dup
ENST00000225275.4:c.1465_1470dup MANE Select	ENSP00000225275.3:p.Ile490_Ala491insArgIle
ENST00000225275.3:c.1465_1470dup	ENSP00000225275.3:p.Ile490_Ala491insArgIle
NM_000250.1:c.1465_1470dup , LRG_84t1:c.1465_1470dup	NP_000241.1:p.Ile490_Ala491insArgIle
XM_011524821.1:c.1651_1656dup	XP_011523123.1:p.Ile552_Ala553insArgIle
XM_011524822.1:c.1180_1185dup	XP_011523124.1:p.Ile395_Ala396insArgIle
XM_011524823.1:c.*14_*19dup	XP_011523125.1:n.*14_*19dup
NM_000250.2:c.1465_1470dup MANE Select	NP_000241.1:p.Ile490_Ala491insArgIle