Canonical Allele Identifier: CA501023623

Gene: MPO

Linked Data

• gnomAD v4: 17-58273649-G-A
• MyVariant Identifiers: chr17:g.56351010G>A (hg19)

Genomic Alleles

HGVS	Genome Assembly
NC_000017.11:g.58273649G>A , CM000679.2:g.58273649G>A	GRCh38
NC_000017.10:g.56351010G>A , CM000679.1:g.56351010G>A	GRCh37
NC_000017.9:g.53706009G>A	NCBI36
NG_009629.1:g.12287C>T , LRG_84:g.12287C>T

Transcript Alleles

HGVS	Amino-acid Change
ENST00000578493.2:n.719C>T
ENST00000699291.1:c.511C>T	ENSP00000514272.1:p.Pro171Ser
ENST00000699292.1:n.426C>T
ENST00000225275.4:c.1386C>T MANE Select	ENSP00000225275.3:p.Tyr462=
ENST00000225275.3:c.1386C>T	ENSP00000225275.3:p.Tyr462=
NM_000250.1:c.1386C>T , LRG_84t1:c.1386C>T	NP_000241.1:p.Tyr462=
XM_011524821.1:c.1572C>T	XP_011523123.1:p.Tyr524=
XM_011524822.1:c.1101C>T	XP_011523124.1:p.Tyr367=
XM_011524823.1:c.1411C>T	XP_011523125.1:p.Pro471Ser
NM_000250.2:c.1386C>T MANE Select	NP_000241.1:p.Tyr462=