Canonical Allele Identifier: CA773505924

Gene: MPO

Linked Data

• dbSNP Id: rs536522394
• MyVariant Identifiers: chr17:g.56350827_56350828insGGGTTGGGTTCCAT (hg19) ; chr17:g.58273466_58273467insGGGTTGGGTTCCAT (hg38)

Genomic Alleles

HGVS	Genome Assembly
NC_000017.11:g.58273470_58273483dup , CM000679.2:g.58273470_58273483dup	GRCh38
NC_000017.10:g.56350831_56350844dup , CM000679.1:g.56350831_56350844dup	GRCh37
NC_000017.9:g.53705830_53705843dup	NCBI36
NG_009629.1:g.12456_12469dup , LRG_84:g.12456_12469dup

Transcript Alleles

HGVS	Amino-acid change
ENST00000578493.2:n.888_901dup
ENST00000699291.1:c.680_693dup	ENSP00000514272.1:n.680_693dup
ENST00000699292.1:n.595_608dup
ENST00000225275.4:c.1555_1568dup MANE Select	ENSP00000225275.3:p.Arg524TrpfsTer?
ENST00000225275.3:c.1555_1568dup	ENSP00000225275.3:p.Arg524TrpfsTer?
ENST00000577220.1:c.13_26dup	ENSP00000464668.1:p.Arg10TrpfsTer?
NM_000250.1:c.1555_1568dup , LRG_84t1:c.1555_1568dup	NP_000241.1:p.Arg524TrpfsTer?
XM_011524821.1:c.1741_1754dup	XP_011523123.1:p.Arg586TrpfsTer?
XM_011524822.1:c.1270_1283dup	XP_011523124.1:p.Arg429TrpfsTer?
XM_011524823.1:c.*104_*117dup	XP_011523125.1:n.*104_*117dup
NM_000250.2:c.1555_1568dup MANE Select	NP_000241.1:p.Arg524TrpfsTer?