Canonical Allele Identifier: CA400369364

Gene: MPO

Linked Data

• MyVariant Identifiers: chr17:g.56350217G>C (hg19) ; chr17:g.58272856G>C (hg38)

Genomic Alleles

HGVS	Genome Assembly
NC_000017.11:g.58272856G>C , CM000679.2:g.58272856G>C	GRCh38
NC_000017.10:g.56350217G>C , CM000679.1:g.56350217G>C	GRCh37
NC_000017.9:g.53705216G>C	NCBI36
NG_009629.1:g.13080C>G , LRG_84:g.13080C>G

Transcript Alleles

HGVS	Amino-acid Change
ENST00000578493.2:n.1017C>G
ENST00000699291.1:c.809C>G	ENSP00000514272.1:n.809C>G
ENST00000699292.1:n.1219C>G
ENST00000225275.4:c.1684C>G MANE Select	ENSP00000225275.3:p.Gln562Glu
ENST00000225275.3:c.1684C>G	ENSP00000225275.3:p.Gln562Glu
ENST00000577220.1:c.142C>G	ENSP00000464668.1:p.Gln48Glu
NM_000250.1:c.1684C>G , LRG_84t1:c.1684C>G	NP_000241.1:p.Gln562Glu
XM_011524821.1:c.1870C>G	XP_011523123.1:p.Gln624Glu
XM_011524822.1:c.1399C>G	XP_011523124.1:p.Gln467Glu
NM_000250.2:c.1684C>G MANE Select	NP_000241.1:p.Gln562Glu