Canonical Allele Identifier: CA400370464

Gene: MPO

Linked Data

• gnomAD v4: 17-58273633-C-T
• MyVariant Identifiers: chr17:g.56350994C>T (hg19) ; chr17:g.58273633C>T (hg38)

Genomic Alleles

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

Transcript Alleles

HGVS	Amino-acid Change
ENST00000578493.2:n.735G>A
ENST00000699291.1:c.527G>A	ENSP00000514272.1:p.Gly176Glu
ENST00000699292.1:n.442G>A
ENST00000225275.4:c.1402G>A MANE Select	ENSP00000225275.3:p.Gly468Arg
ENST00000225275.3:c.1402G>A	ENSP00000225275.3:p.Gly468Arg
NM_000250.1:c.1402G>A , LRG_84t1:c.1402G>A	NP_000241.1:p.Gly468Arg
XM_011524821.1:c.1588G>A	XP_011523123.1:p.Gly530Arg
XM_011524822.1:c.1117G>A	XP_011523124.1:p.Gly373Arg
XM_011524823.1:c.1427G>A	XP_011523125.1:p.Gly476Glu
NM_000250.2:c.1402G>A MANE Select	NP_000241.1:p.Gly468Arg