Canonical Allele Identifier: CA626724240

Gene: MPO

Linked Data

• dbSNP Id: rs1422424531
• gnomAD v2: 17-56351048-G-T
• gnomAD v4: 17-58273687-G-T
• MyVariant Identifiers: chr17:g.56351048G>T (hg19) ; chr17:g.58273687G>T (hg38)

Genomic Alleles

HGVS	Genome Assembly
NC_000017.11:g.58273687G>T , CM000679.2:g.58273687G>T	GRCh38
NC_000017.10:g.56351048G>T , CM000679.1:g.56351048G>T	GRCh37
NC_000017.9:g.53706047G>T	NCBI36
NG_009629.1:g.12249C>A , LRG_84:g.12249C>A

Transcript Alleles

HGVS	Amino-acid Change
ENST00000578493.2:n.699-18C>A
ENST00000699291.1:c.491-18C>A	ENSP00000514272.1:n.491-18C>A
ENST00000699292.1:n.388C>A
ENST00000225275.4:c.1366-18C>A MANE Select	ENSP00000225275.3:n.1366-18C>A
ENST00000225275.3:c.1366-18C>A	ENSP00000225275.3:n.1366-18C>A
NM_000250.1:c.1366-18C>A , LRG_84t1:c.1366-18C>A	NP_000241.1:n.1366-18C>A
XM_011524821.1:c.1552-18C>A	XP_011523123.1:n.1552-18C>A
XM_011524822.1:c.1081-18C>A	XP_011523124.1:n.1081-18C>A
XM_011524823.1:c.1391-18C>A	XP_011523125.1:n.1391-18C>A
NM_000250.2:c.1366-18C>A MANE Select	NP_000241.1:n.1366-18C>A