Canonical Allele Identifier: CA292011798

Gene: MPO

Linked Data

• dbSNP Id: rs966801133
• gnomAD v2: 17-56350036-AG-A
• gnomAD v3: 17-58272675-AG-A
• gnomAD v4: 17-58272675-AG-A
• MyVariant Identifiers: chr17:g.56350037del (hg19) ; chr17:g.58272676del (hg38)

Genomic Alleles

HGVS	Genome Assembly
NC_000017.11:g.58272681del , CM000679.2:g.58272681del	GRCh38
NC_000017.10:g.56350042del , CM000679.1:g.56350042del	GRCh37
NC_000017.9:g.53705041del	NCBI36
NG_009629.1:g.13260del , LRG_84:g.13260del

Transcript Alleles

HGVS	Amino-acid Change
ENST00000578493.2:n.1125+72del
ENST00000699291.1:c.917+72del	ENSP00000514272.1:n.917+72del
ENST00000699292.1:n.1327+72del
ENST00000225275.4:c.1792+72del MANE Select	ENSP00000225275.3:n.1792+72del
ENST00000225275.3:c.1792+72del	ENSP00000225275.3:n.1792+72del
ENST00000577220.1:c.183+139del	ENSP00000464668.1:n.183+139del
NM_000250.1:c.1792+72del , LRG_84t1:c.1792+72del	NP_000241.1:n.1792+72del
XM_011524821.1:c.1978+72del	XP_011523123.1:n.1978+72del
XM_011524822.1:c.1507+72del	XP_011523124.1:n.1507+72del
NM_000250.2:c.1792+72del MANE Select	NP_000241.1:n.1792+72del