Canonical Allele Identifier: CA400370458

Gene: MPO

Linked Data

• MyVariant Identifiers: chr17:g.56350993C>G (hg19) ; chr17:g.58273632C>G (hg38)

Genomic Alleles

HGVS	Genome Assembly
NC_000017.11:g.58273632C>G , CM000679.2:g.58273632C>G	GRCh38
NC_000017.10:g.56350993C>G , CM000679.1:g.56350993C>G	GRCh37
NC_000017.9:g.53705992C>G	NCBI36
NG_009629.1:g.12304G>C , LRG_84:g.12304G>C

Transcript Alleles

HGVS	Amino-acid Change
ENST00000578493.2:n.736G>C
ENST00000699291.1:c.528G>C	ENSP00000514272.1:p.Gly176=
ENST00000699292.1:n.443G>C
ENST00000225275.4:c.1403G>C MANE Select	ENSP00000225275.3:p.Gly468Ala
ENST00000225275.3:c.1403G>C	ENSP00000225275.3:p.Gly468Ala
NM_000250.1:c.1403G>C , LRG_84t1:c.1403G>C	NP_000241.1:p.Gly468Ala
XM_011524821.1:c.1589G>C	XP_011523123.1:p.Gly530Ala
XM_011524822.1:c.1118G>C	XP_011523124.1:p.Gly373Ala
XM_011524823.1:c.1428G>C	XP_011523125.1:p.Gly476=
NM_000250.2:c.1403G>C MANE Select	NP_000241.1:p.Gly468Ala