Canonical Allele Identifier: CA773506109

Gene: MPO

Linked Data

• dbSNP Id: rs1380036982
• MyVariant Identifiers: chr17:g.56350924_56350928del (hg19) ; chr17:g.58273563_58273567del (hg38)

Genomic Alleles

HGVS	Genome Assembly
NC_000017.11:g.58273566_58273570del , CM000679.2:g.58273566_58273570del	GRCh38
NC_000017.10:g.56350927_56350931del , CM000679.1:g.56350927_56350931del	GRCh37
NC_000017.9:g.53705926_53705930del	NCBI36
NG_009629.1:g.12369_12373del , LRG_84:g.12369_12373del

Transcript Alleles

HGVS	Amino-acid Change
ENST00000578493.2:n.801_805del
ENST00000699291.1:c.593_597del	ENSP00000514272.1:n.593_597del
ENST00000699292.1:n.508_512del
ENST00000225275.4:c.1468_1472del MANE Select	ENSP00000225275.3:p.Ile490GlnfsTer?
ENST00000225275.3:c.1468_1472del	ENSP00000225275.3:p.Ile490GlnfsTer?
NM_000250.1:c.1468_1472del , LRG_84t1:c.1468_1472del	NP_000241.1:p.Ile490GlnfsTer?
XM_011524821.1:c.1654_1658del	XP_011523123.1:p.Ile552GlnfsTer?
XM_011524822.1:c.1183_1187del	XP_011523124.1:p.Ile395GlnfsTer?
XM_011524823.1:c.*17_*21del	XP_011523125.1:n.*17_*21del
NM_000250.2:c.1468_1472del MANE Select	NP_000241.1:p.Ile490GlnfsTer?