Canonical Allele Identifier: CA501022192

Gene: MPO

Linked Data

• MyVariant Identifiers: chr17:g.56350803A>G (hg19)

Genomic Alleles

HGVS	Genome Assembly
NC_000017.11:g.58273442A>G , CM000679.2:g.58273442A>G	GRCh38
NC_000017.10:g.56350803A>G , CM000679.1:g.56350803A>G	GRCh37
NC_000017.9:g.53705802A>G	NCBI36
NG_009629.1:g.12494T>C , LRG_84:g.12494T>C

Transcript Alleles

HGVS	Amino-acid Change
ENST00000578493.2:n.926T>C
ENST00000699291.1:c.718T>C	ENSP00000514272.1:n.718T>C
ENST00000699292.1:n.633T>C
ENST00000225275.4:c.1593T>C MANE Select	ENSP00000225275.3:p.Phe531=
ENST00000225275.3:c.1593T>C	ENSP00000225275.3:p.Phe531=
ENST00000577220.1:c.51T>C	ENSP00000464668.1:p.Phe17=
NM_000250.1:c.1593T>C , LRG_84t1:c.1593T>C	NP_000241.1:p.Phe531=
XM_011524821.1:c.1779T>C	XP_011523123.1:p.Phe593=
XM_011524822.1:c.1308T>C	XP_011523124.1:p.Phe436=
XM_011524823.1:c.*142T>C	XP_011523125.1:n.*142T>C
NM_000250.2:c.1593T>C MANE Select	NP_000241.1:p.Phe531=