Canonical Allele Identifier: CA501023040

Gene: MPO

Linked Data

• MyVariant Identifiers: chr17:g.56350956A>C (hg19)

Genomic Alleles

HGVS	Genome Assembly
NC_000017.11:g.58273595A>C , CM000679.2:g.58273595A>C	GRCh38
NC_000017.10:g.56350956A>C , CM000679.1:g.56350956A>C	GRCh37
NC_000017.9:g.53705955A>C	NCBI36
NG_009629.1:g.12341T>G , LRG_84:g.12341T>G

Transcript Alleles

HGVS	Amino-acid Change
ENST00000578493.2:n.773T>G
ENST00000699291.1:c.565T>G	ENSP00000514272.1:p.Phe189Val
ENST00000699292.1:n.480T>G
ENST00000225275.4:c.1440T>G MANE Select	ENSP00000225275.3:p.Arg480=
ENST00000225275.3:c.1440T>G	ENSP00000225275.3:p.Arg480=
NM_000250.1:c.1440T>G , LRG_84t1:c.1440T>G	NP_000241.1:p.Arg480=
XM_011524821.1:c.1626T>G	XP_011523123.1:p.Arg542=
XM_011524822.1:c.1155T>G	XP_011523124.1:p.Arg385=
XM_011524823.1:c.1465T>G	XP_011523125.1:p.Phe489Val
NM_000250.2:c.1440T>G MANE Select	NP_000241.1:p.Arg480=