Canonical Allele Identifier: CA656667138

Gene: MPO

Linked Data

• COSMIC: COSN20943925

Genomic Alleles

HGVS	Genome Assembly
NC_000017.11:g.58273680G>T , CM000679.2:g.58273680G>T	GRCh38
NC_000017.10:g.56351041G>T , CM000679.1:g.56351041G>T	GRCh37
NC_000017.9:g.53706040G>T	NCBI36
NG_009629.1:g.12256C>A , LRG_84:g.12256C>A

Transcript Alleles

HGVS	Amino-acid Change
ENST00000578493.2:n.699-11C>A
ENST00000699291.1:c.491-11C>A	ENSP00000514272.1:n.491-11C>A
ENST00000699292.1:n.395C>A
ENST00000225275.4:c.1366-11C>A MANE Select	ENSP00000225275.3:n.1366-11C>A
ENST00000225275.3:c.1366-11C>A	ENSP00000225275.3:n.1366-11C>A
NM_000250.1:c.1366-11C>A , LRG_84t1:c.1366-11C>A	NP_000241.1:n.1366-11C>A
XM_011524821.1:c.1552-11C>A	XP_011523123.1:n.1552-11C>A
XM_011524822.1:c.1081-11C>A	XP_011523124.1:n.1081-11C>A
XM_011524823.1:c.1391-11C>A	XP_011523125.1:n.1391-11C>A
NM_000250.2:c.1366-11C>A MANE Select	NP_000241.1:n.1366-11C>A