Canonical Allele Identifier: CA400370106

Gene: MPO

Linked Data

• MyVariant Identifiers: chr17:g.56350892G>C (hg19) ; chr17:g.58273531G>C (hg38)

Genomic Alleles

HGVS	Genome Assembly
NC_000017.11:g.58273531G>C , CM000679.2:g.58273531G>C	GRCh38
NC_000017.10:g.56350892G>C , CM000679.1:g.56350892G>C	GRCh37
NC_000017.9:g.53705891G>C	NCBI36
NG_009629.1:g.12405C>G , LRG_84:g.12405C>G

Transcript Alleles

HGVS	Amino-acid Change
ENST00000578493.2:n.837C>G
ENST00000699291.1:c.629C>G	ENSP00000514272.1:n.629C>G
ENST00000699292.1:n.544C>G
ENST00000225275.4:c.1504C>G MANE Select	ENSP00000225275.3:p.His502Asp
ENST00000225275.3:c.1504C>G	ENSP00000225275.3:p.His502Asp
NM_000250.1:c.1504C>G , LRG_84t1:c.1504C>G	NP_000241.1:p.His502Asp
XM_011524821.1:c.1690C>G	XP_011523123.1:p.His564Asp
XM_011524822.1:c.1219C>G	XP_011523124.1:p.His407Asp
XM_011524823.1:c.*53C>G	XP_011523125.1:n.*53C>G
NM_000250.2:c.1504C>G MANE Select	NP_000241.1:p.His502Asp