Canonical Allele Identifier: CA400370462

Gene: MPO

Linked Data

• MyVariant Identifiers: chr17:g.56350994C>A (hg19) ; chr17:g.58273633C>A (hg38)

Genomic Alleles

HGVS	Genome Assembly
NC_000017.11:g.58273633C>A , CM000679.2:g.58273633C>A	GRCh38
NC_000017.10:g.56350994C>A , CM000679.1:g.56350994C>A	GRCh37
NC_000017.9:g.53705993C>A	NCBI36
NG_009629.1:g.12303G>T , LRG_84:g.12303G>T

Transcript Alleles

HGVS	Amino-acid Change
ENST00000578493.2:n.735G>T
ENST00000699291.1:c.527G>T	ENSP00000514272.1:p.Gly176Val
ENST00000699292.1:n.442G>T
ENST00000225275.4:c.1402G>T MANE Select	ENSP00000225275.3:p.Gly468Trp
ENST00000225275.3:c.1402G>T	ENSP00000225275.3:p.Gly468Trp
NM_000250.1:c.1402G>T , LRG_84t1:c.1402G>T	NP_000241.1:p.Gly468Trp
XM_011524821.1:c.1588G>T	XP_011523123.1:p.Gly530Trp
XM_011524822.1:c.1117G>T	XP_011523124.1:p.Gly373Trp
XM_011524823.1:c.1427G>T	XP_011523125.1:p.Gly476Val
NM_000250.2:c.1402G>T MANE Select	NP_000241.1:p.Gly468Trp