Canonical Allele Identifier: CA400366031

Gene: MPO

Linked Data

• MyVariant Identifiers: chr17:g.56348133C>G (hg19) ; chr17:g.58270772C>G (hg38)

Genomic Alleles

HGVS	Genome Assembly
NC_000017.11:g.58270772C>G , CM000679.2:g.58270772C>G	GRCh38
NC_000017.10:g.56348133C>G , CM000679.1:g.56348133C>G	GRCh37
NC_000017.9:g.53703132C>G	NCBI36
NG_009629.1:g.15164G>C , LRG_84:g.15164G>C

Transcript Alleles

HGVS	Amino-acid change
ENST00000578493.2:n.1455G>C
ENST00000699291.1:c.1247G>C	ENSP00000514272.1:n.1247G>C
ENST00000699292.1:n.1657G>C
ENST00000225275.4:c.2122G>C MANE Select	ENSP00000225275.3:p.Gly708Arg
ENST00000225275.3:c.2122G>C	ENSP00000225275.3:p.Gly708Arg
ENST00000577220.1:c.217G>C	ENSP00000464668.1:p.Gly73Arg
NM_000250.1:c.2122G>C , LRG_84t1:c.2122G>C	NP_000241.1:p.Gly708Arg
XM_011524821.1:c.2308G>C	XP_011523123.1:p.Gly770Arg
XM_011524822.1:c.1837G>C	XP_011523124.1:p.Gly613Arg
NM_000250.2:c.2122G>C MANE Select	NP_000241.1:p.Gly708Arg