Canonical Allele Identifier: CA400370308

Gene: MPO

Linked Data

• MyVariant Identifiers: chr17:g.56350949T>G (hg19) ; chr17:g.58273588T>G (hg38)

Genomic Alleles

HGVS	Genome Assembly
NC_000017.11:g.58273588T>G , CM000679.2:g.58273588T>G	GRCh38
NC_000017.10:g.56350949T>G , CM000679.1:g.56350949T>G	GRCh37
NC_000017.9:g.53705948T>G	NCBI36
NG_009629.1:g.12348A>C , LRG_84:g.12348A>C

Transcript Alleles

HGVS	Amino-acid Change
ENST00000578493.2:n.780A>C
ENST00000699291.1:c.572A>C	ENSP00000514272.1:p.Gln191Pro
ENST00000699292.1:n.487A>C
ENST00000225275.4:c.1447A>C MANE Select	ENSP00000225275.3:p.Asn483His
ENST00000225275.3:c.1447A>C	ENSP00000225275.3:p.Asn483His
NM_000250.1:c.1447A>C , LRG_84t1:c.1447A>C	NP_000241.1:p.Asn483His
XM_011524821.1:c.1633A>C	XP_011523123.1:p.Asn545His
XM_011524822.1:c.1162A>C	XP_011523124.1:p.Asn388His
XM_011524823.1:c.1472A>C	XP_011523125.1:p.Gln491Pro
NM_000250.2:c.1447A>C MANE Select	NP_000241.1:p.Asn483His