Canonical Allele Identifier: CA400370020

Gene: MPO

Linked Data

• MyVariant Identifiers: chr17:g.56350877G>T (hg19) ; chr17:g.58273516G>T (hg38)

Genomic Alleles

HGVS	Genome Assembly
NC_000017.11:g.58273516G>T , CM000679.2:g.58273516G>T	GRCh38
NC_000017.10:g.56350877G>T , CM000679.1:g.56350877G>T	GRCh37
NC_000017.9:g.53705876G>T	NCBI36
NG_009629.1:g.12420C>A , LRG_84:g.12420C>A

Transcript Alleles

HGVS	Amino-acid Change
ENST00000578493.2:n.852C>A
ENST00000699291.1:c.644C>A	ENSP00000514272.1:n.644C>A
ENST00000699292.1:n.559C>A
ENST00000225275.4:c.1519C>A MANE Select	ENSP00000225275.3:p.Pro507Thr
ENST00000225275.3:c.1519C>A	ENSP00000225275.3:p.Pro507Thr
NM_000250.1:c.1519C>A , LRG_84t1:c.1519C>A	NP_000241.1:p.Pro507Thr
XM_011524821.1:c.1705C>A	XP_011523123.1:p.Pro569Thr
XM_011524822.1:c.1234C>A	XP_011523124.1:p.Pro412Thr
XM_011524823.1:c.*68C>A	XP_011523125.1:n.*68C>A
NM_000250.2:c.1519C>A MANE Select	NP_000241.1:p.Pro507Thr