Canonical Allele Identifier: CA400369387

Gene: MPO

Linked Data

• MyVariant Identifiers: chr17:g.56350222T>C (hg19) ; chr17:g.58272861T>C (hg38)

Genomic Alleles

HGVS	Genome Assembly
NC_000017.11:g.58272861T>C , CM000679.2:g.58272861T>C	GRCh38
NC_000017.10:g.56350222T>C , CM000679.1:g.56350222T>C	GRCh37
NC_000017.9:g.53705221T>C	NCBI36
NG_009629.1:g.13075A>G , LRG_84:g.13075A>G

Transcript Alleles

HGVS	Amino-acid Change
ENST00000578493.2:n.1012A>G
ENST00000699291.1:c.804A>G	ENSP00000514272.1:n.804A>G
ENST00000699292.1:n.1214A>G
ENST00000225275.4:c.1679A>G MANE Select	ENSP00000225275.3:p.Gln560Arg
ENST00000225275.3:c.1679A>G	ENSP00000225275.3:p.Gln560Arg
ENST00000577220.1:c.137A>G	ENSP00000464668.1:p.Gln46Arg
NM_000250.1:c.1679A>G , LRG_84t1:c.1679A>G	NP_000241.1:p.Gln560Arg
XM_011524821.1:c.1865A>G	XP_011523123.1:p.Gln622Arg
XM_011524822.1:c.1394A>G	XP_011523124.1:p.Gln465Arg
NM_000250.2:c.1679A>G MANE Select	NP_000241.1:p.Gln560Arg