Canonical Allele Identifier: CA501022054

Gene: MPO

Linked Data

• MyVariant Identifiers: chr17:g.56350776T>C (hg19)

Genomic Alleles

HGVS	Genome Assembly
NC_000017.11:g.58273415T>C , CM000679.2:g.58273415T>C	GRCh38
NC_000017.10:g.56350776T>C , CM000679.1:g.56350776T>C	GRCh37
NC_000017.9:g.53705775T>C	NCBI36
NG_009629.1:g.12521A>G , LRG_84:g.12521A>G

Transcript Alleles

HGVS	Amino-acid change
ENST00000578493.2:n.953A>G
ENST00000699291.1:c.745A>G	ENSP00000514272.1:n.745A>G
ENST00000699292.1:n.660A>G
ENST00000225275.4:c.1620A>G MANE Select	ENSP00000225275.3:p.Glu540=
ENST00000225275.3:c.1620A>G	ENSP00000225275.3:p.Glu540=
ENST00000577220.1:c.78A>G	ENSP00000464668.1:p.Glu26=
NM_000250.1:c.1620A>G , LRG_84t1:c.1620A>G	NP_000241.1:p.Glu540=
XM_011524821.1:c.1806A>G	XP_011523123.1:p.Glu602=
XM_011524822.1:c.1335A>G	XP_011523124.1:p.Glu445=
NM_000250.2:c.1620A>G MANE Select	NP_000241.1:p.Glu540=