Canonical Allele Identifier: CA2638969150

Gene: MPO

Linked Data

• gnomAD v4: 17-58273684-T-A

Genomic Alleles

HGVS	Genome Assembly
NC_000017.11:g.58273684T>A , CM000679.2:g.58273684T>A	GRCh38
NC_000017.10:g.56351045T>A , CM000679.1:g.56351045T>A	GRCh37
NC_000017.9:g.53706044T>A	NCBI36
NG_009629.1:g.12252A>T , LRG_84:g.12252A>T

Transcript Alleles

HGVS	Amino-acid Change
ENST00000578493.2:n.699-15A>T
ENST00000699291.1:c.491-15A>T	ENSP00000514272.1:n.491-15A>T
ENST00000699292.1:n.391A>T
ENST00000225275.4:c.1366-15A>T MANE Select	ENSP00000225275.3:n.1366-15A>T
ENST00000225275.3:c.1366-15A>T	ENSP00000225275.3:n.1366-15A>T
NM_000250.1:c.1366-15A>T , LRG_84t1:c.1366-15A>T	NP_000241.1:n.1366-15A>T
XM_011524821.1:c.1552-15A>T	XP_011523123.1:n.1552-15A>T
XM_011524822.1:c.1081-15A>T	XP_011523124.1:n.1081-15A>T
XM_011524823.1:c.1391-15A>T	XP_011523125.1:n.1391-15A>T
NM_000250.2:c.1366-15A>T MANE Select	NP_000241.1:n.1366-15A>T