Canonical Allele Identifier: CA400369379

Gene: MPO

Linked Data

• MyVariant Identifiers: chr17:g.56350220T>C (hg19) ; chr17:g.58272859T>C (hg38)

Genomic Alleles

HGVS	Genome Assembly
NC_000017.11:g.58272859T>C , CM000679.2:g.58272859T>C	GRCh38
NC_000017.10:g.56350220T>C , CM000679.1:g.56350220T>C	GRCh37
NC_000017.9:g.53705219T>C	NCBI36
NG_009629.1:g.13077A>G , LRG_84:g.13077A>G

Transcript Alleles

HGVS	Amino-acid Change
ENST00000578493.2:n.1014A>G
ENST00000699291.1:c.806A>G	ENSP00000514272.1:n.806A>G
ENST00000699292.1:n.1216A>G
ENST00000225275.4:c.1681A>G MANE Select	ENSP00000225275.3:p.Asn561Asp
ENST00000225275.3:c.1681A>G	ENSP00000225275.3:p.Asn561Asp
ENST00000577220.1:c.139A>G	ENSP00000464668.1:p.Asn47Asp
NM_000250.1:c.1681A>G , LRG_84t1:c.1681A>G	NP_000241.1:p.Asn561Asp
XM_011524821.1:c.1867A>G	XP_011523123.1:p.Asn623Asp
XM_011524822.1:c.1396A>G	XP_011523124.1:p.Asn466Asp
NM_000250.2:c.1681A>G MANE Select	NP_000241.1:p.Asn561Asp