Canonical Allele Identifier: CA400369290

Gene: MPO

Linked Data

• MyVariant Identifiers: chr17:g.56350201T>C (hg19) ; chr17:g.58272840T>C (hg38)

Genomic Alleles

HGVS	Genome Assembly
NC_000017.11:g.58272840T>C , CM000679.2:g.58272840T>C	GRCh38
NC_000017.10:g.56350201T>C , CM000679.1:g.56350201T>C	GRCh37
NC_000017.9:g.53705200T>C	NCBI36
NG_009629.1:g.13096A>G , LRG_84:g.13096A>G

Transcript Alleles

HGVS	Amino-acid change
ENST00000578493.2:n.1033A>G
ENST00000699291.1:c.825A>G	ENSP00000514272.1:n.825A>G
ENST00000699292.1:n.1235A>G
ENST00000225275.4:c.1700A>G MANE Select	ENSP00000225275.3:p.Glu567Gly
ENST00000225275.3:c.1700A>G	ENSP00000225275.3:p.Glu567Gly
ENST00000577220.1:c.158A>G	ENSP00000464668.1:p.Glu53Gly
NM_000250.1:c.1700A>G , LRG_84t1:c.1700A>G	NP_000241.1:p.Glu567Gly
XM_011524821.1:c.1886A>G	XP_011523123.1:p.Glu629Gly
XM_011524822.1:c.1415A>G	XP_011523124.1:p.Glu472Gly
NM_000250.2:c.1700A>G MANE Select	NP_000241.1:p.Glu567Gly