Canonical Allele Identifier: CA400370519

Gene: MPO

Linked Data

• COSMIC: COSM3362244 ; COSM3362245
• MyVariant Identifiers: chr17:g.56351014T>C (hg19) ; chr17:g.58273653T>C (hg38)

Genomic Alleles

HGVS	Genome Assembly
NC_000017.11:g.58273653T>C , CM000679.2:g.58273653T>C	GRCh38
NC_000017.10:g.56351014T>C , CM000679.1:g.56351014T>C	GRCh37
NC_000017.9:g.53706013T>C	NCBI36
NG_009629.1:g.12283A>G , LRG_84:g.12283A>G

Transcript Alleles

HGVS	Amino-acid Change
ENST00000578493.2:n.715A>G
ENST00000699291.1:c.507A>G	ENSP00000514272.1:p.Gly169=
ENST00000699292.1:n.422A>G
ENST00000225275.4:c.1382A>G MANE Select	ENSP00000225275.3:p.Asp461Gly
ENST00000225275.3:c.1382A>G	ENSP00000225275.3:p.Asp461Gly
NM_000250.1:c.1382A>G , LRG_84t1:c.1382A>G	NP_000241.1:p.Asp461Gly
XM_011524821.1:c.1568A>G	XP_011523123.1:p.Asp523Gly
XM_011524822.1:c.1097A>G	XP_011523124.1:p.Asp366Gly
XM_011524823.1:c.1407A>G	XP_011523125.1:p.Gly469=
NM_000250.2:c.1382A>G MANE Select	NP_000241.1:p.Asp461Gly