Canonical Allele Identifier: CA400370117

Gene: MPO

Linked Data

• MyVariant Identifiers: chr17:g.56350894C>T (hg19) ; chr17:g.58273533C>T (hg38)

Genomic Alleles

HGVS	Genome Assembly
NC_000017.11:g.58273533C>T , CM000679.2:g.58273533C>T	GRCh38
NC_000017.10:g.56350894C>T , CM000679.1:g.56350894C>T	GRCh37
NC_000017.9:g.53705893C>T	NCBI36
NG_009629.1:g.12403G>A , LRG_84:g.12403G>A

Transcript Alleles

HGVS	Amino-acid Change
ENST00000578493.2:n.835G>A
ENST00000699291.1:c.627G>A	ENSP00000514272.1:n.627G>A
ENST00000699292.1:n.542G>A
ENST00000225275.4:c.1502G>A MANE Select	ENSP00000225275.3:p.Gly501Asp
ENST00000225275.3:c.1502G>A	ENSP00000225275.3:p.Gly501Asp
NM_000250.1:c.1502G>A , LRG_84t1:c.1502G>A	NP_000241.1:p.Gly501Asp
XM_011524821.1:c.1688G>A	XP_011523123.1:p.Gly563Asp
XM_011524822.1:c.1217G>A	XP_011523124.1:p.Gly406Asp
XM_011524823.1:c.*51G>A	XP_011523125.1:n.*51G>A
NM_000250.2:c.1502G>A MANE Select	NP_000241.1:p.Gly501Asp