Canonical Allele Identifier: CA292012271

Gene: MPO

Linked Data

• dbSNP Id: rs200746810
• MyVariant Identifiers: chr17:g.56350893G>A (hg19) ; chr17:g.58273532G>A (hg38)

Genomic Alleles

HGVS	Genome Assembly
NC_000017.11:g.58273532G>A , CM000679.2:g.58273532G>A	GRCh38
NC_000017.10:g.56350893G>A , CM000679.1:g.56350893G>A	GRCh37
NC_000017.9:g.53705892G>A	NCBI36
NG_009629.1:g.12404C>T , LRG_84:g.12404C>T

Transcript Alleles

HGVS	Amino-acid Change
ENST00000578493.2:n.836C>T
ENST00000699291.1:c.628C>T	ENSP00000514272.1:n.628C>T
ENST00000699292.1:n.543C>T
ENST00000225275.4:c.1503C>T MANE Select	ENSP00000225275.3:p.Gly501=
ENST00000225275.3:c.1503C>T	ENSP00000225275.3:p.Gly501=
NM_000250.1:c.1503C>T , LRG_84t1:c.1503C>T	NP_000241.1:p.Gly501=
XM_011524821.1:c.1689C>T	XP_011523123.1:p.Gly563=
XM_011524822.1:c.1218C>T	XP_011523124.1:p.Gly406=
XM_011524823.1:c.*52C>T	XP_011523125.1:n.*52C>T
NM_000250.2:c.1503C>T MANE Select	NP_000241.1:p.Gly501=