Canonical Allele Identifier: CA773481971

Gene: MPO

Linked Data

• dbSNP Id: rs1302202817
• MyVariant Identifiers: chr17:g.56351063_56351069del (hg19) ; chr17:g.58273702_58273708del (hg38)

Genomic Alleles

HGVS	Genome Assembly
NC_000017.11:g.58273703_58273709del , CM000679.2:g.58273703_58273709del	GRCh38
NC_000017.10:g.56351064_56351070del , CM000679.1:g.56351064_56351070del	GRCh37
NC_000017.9:g.53706063_53706069del	NCBI36
NG_009629.1:g.12228_12234del , LRG_84:g.12228_12234del

Transcript Alleles

HGVS	Amino-acid Change
ENST00000578493.2:n.699-39_699-33del
ENST00000699291.1:c.491-39_491-33del	ENSP00000514272.1:n.491-39_491-33del
ENST00000699292.1:n.367_373del
ENST00000225275.4:c.1366-39_1366-33del MANE Select	ENSP00000225275.3:n.1366-39_1366-33del
ENST00000225275.3:c.1366-39_1366-33del	ENSP00000225275.3:n.1366-39_1366-33del
NM_000250.1:c.1366-39_1366-33del , LRG_84t1:c.1366-39_1366-33del	NP_000241.1:n.1366-39_1366-33del
XM_011524821.1:c.1552-39_1552-33del	XP_011523123.1:n.1552-39_1552-33del
XM_011524822.1:c.1081-39_1081-33del	XP_011523124.1:n.1081-39_1081-33del
XM_011524823.1:c.1391-39_1391-33del	XP_011523125.1:n.1391-39_1391-33del
NM_000250.2:c.1366-39_1366-33del MANE Select	NP_000241.1:n.1366-39_1366-33del