Canonical Allele Identifier: CA501022823

Gene: MPO

Linked Data

• MyVariant Identifiers: chr17:g.56350911G>A (hg19)

Genomic Alleles

HGVS	Genome Assembly
NC_000017.11:g.58273550G>A , CM000679.2:g.58273550G>A	GRCh38
NC_000017.10:g.56350911G>A , CM000679.1:g.56350911G>A	GRCh37
NC_000017.9:g.53705910G>A	NCBI36
NG_009629.1:g.12386C>T , LRG_84:g.12386C>T

Transcript Alleles

HGVS	Amino-acid Change
ENST00000578493.2:n.818C>T
ENST00000699291.1:c.610C>T	ENSP00000514272.1:n.610C>T
ENST00000699292.1:n.525C>T
ENST00000225275.4:c.1485C>T MANE Select	ENSP00000225275.3:p.Thr495=
ENST00000225275.3:c.1485C>T	ENSP00000225275.3:p.Thr495=
NM_000250.1:c.1485C>T , LRG_84t1:c.1485C>T	NP_000241.1:p.Thr495=
XM_011524821.1:c.1671C>T	XP_011523123.1:p.Thr557=
XM_011524822.1:c.1200C>T	XP_011523124.1:p.Thr400=
XM_011524823.1:c.*34C>T	XP_011523125.1:n.*34C>T
NM_000250.2:c.1485C>T MANE Select	NP_000241.1:p.Thr495=