Canonical Allele Identifier: CA773481960

Gene: MPO

Linked Data

• dbSNP Id: rs1285121296
• gnomAD v3: 17-58273693-G-T
• gnomAD v4: 17-58273693-G-T
• MyVariant Identifiers: chr17:g.56351054G>T (hg19) ; chr17:g.58273693G>T (hg38)

Genomic Alleles

HGVS	Genome Assembly
NC_000017.11:g.58273693G>T , CM000679.2:g.58273693G>T	GRCh38
NC_000017.10:g.56351054G>T , CM000679.1:g.56351054G>T	GRCh37
NC_000017.9:g.53706053G>T	NCBI36
NG_009629.1:g.12243C>A , LRG_84:g.12243C>A

Transcript Alleles

HGVS	Amino-acid Change
ENST00000578493.2:n.699-24C>A
ENST00000699291.1:c.491-24C>A	ENSP00000514272.1:n.491-24C>A
ENST00000699292.1:n.382C>A
ENST00000225275.4:c.1366-24C>A MANE Select	ENSP00000225275.3:n.1366-24C>A
ENST00000225275.3:c.1366-24C>A	ENSP00000225275.3:n.1366-24C>A
NM_000250.1:c.1366-24C>A , LRG_84t1:c.1366-24C>A	NP_000241.1:n.1366-24C>A
XM_011524821.1:c.1552-24C>A	XP_011523123.1:n.1552-24C>A
XM_011524822.1:c.1081-24C>A	XP_011523124.1:n.1081-24C>A
XM_011524823.1:c.1391-24C>A	XP_011523125.1:n.1391-24C>A
NM_000250.2:c.1366-24C>A MANE Select	NP_000241.1:n.1366-24C>A