Canonical Allele Identifier: CA501022980

Gene: MPO

Linked Data

• MyVariant Identifiers: chr17:g.56350941T>G (hg19)

Genomic Alleles

HGVS	Genome Assembly
NC_000017.11:g.58273580T>G , CM000679.2:g.58273580T>G	GRCh38
NC_000017.10:g.56350941T>G , CM000679.1:g.56350941T>G	GRCh37
NC_000017.9:g.53705940T>G	NCBI36
NG_009629.1:g.12356A>C , LRG_84:g.12356A>C

Transcript Alleles

HGVS	Amino-acid Change
ENST00000578493.2:n.788A>C
ENST00000699291.1:c.580A>C	ENSP00000514272.1:n.580A>C
ENST00000699292.1:n.495A>C
ENST00000225275.4:c.1455A>C MANE Select	ENSP00000225275.3:p.Ser485=
ENST00000225275.3:c.1455A>C	ENSP00000225275.3:p.Ser485=
NM_000250.1:c.1455A>C , LRG_84t1:c.1455A>C	NP_000241.1:p.Ser485=
XM_011524821.1:c.1641A>C	XP_011523123.1:p.Ser547=
XM_011524822.1:c.1170A>C	XP_011523124.1:p.Ser390=
XM_011524823.1:c.*4A>C	XP_011523125.1:n.*4A>C
NM_000250.2:c.1455A>C MANE Select	NP_000241.1:p.Ser485=