Canonical Allele Identifier: CA501023539

Gene: MPO

Linked Data

• MyVariant Identifiers: chr17:g.56350995C>G (hg19)

Genomic Alleles

HGVS	Genome Assembly
NC_000017.11:g.58273634C>G , CM000679.2:g.58273634C>G	GRCh38
NC_000017.10:g.56350995C>G , CM000679.1:g.56350995C>G	GRCh37
NC_000017.9:g.53705994C>G	NCBI36
NG_009629.1:g.12302G>C , LRG_84:g.12302G>C

Transcript Alleles

HGVS	Amino-acid Change
ENST00000578493.2:n.734G>C
ENST00000699291.1:c.526G>C	ENSP00000514272.1:p.Gly176Arg
ENST00000699292.1:n.441G>C
ENST00000225275.4:c.1401G>C MANE Select	ENSP00000225275.3:p.Leu467=
ENST00000225275.3:c.1401G>C	ENSP00000225275.3:p.Leu467=
NM_000250.1:c.1401G>C , LRG_84t1:c.1401G>C	NP_000241.1:p.Leu467=
XM_011524821.1:c.1587G>C	XP_011523123.1:p.Leu529=
XM_011524822.1:c.1116G>C	XP_011523124.1:p.Leu372=
XM_011524823.1:c.1426G>C	XP_011523125.1:p.Gly476Arg
NM_000250.2:c.1401G>C MANE Select	NP_000241.1:p.Leu467=