Canonical Allele Identifier: CA501022951

Gene: MPO

Linked Data

• MyVariant Identifiers: chr17:g.56350938C>G (hg19)

Genomic Alleles

HGVS	Genome Assembly
NC_000017.11:g.58273577C>G , CM000679.2:g.58273577C>G	GRCh38
NC_000017.10:g.56350938C>G , CM000679.1:g.56350938C>G	GRCh37
NC_000017.9:g.53705937C>G	NCBI36
NG_009629.1:g.12359G>C , LRG_84:g.12359G>C

Transcript Alleles

HGVS	Amino-acid Change
ENST00000578493.2:n.791G>C
ENST00000699291.1:c.583G>C	ENSP00000514272.1:n.583G>C
ENST00000699292.1:n.498G>C
ENST00000225275.4:c.1458G>C MANE Select	ENSP00000225275.3:p.Val486=
ENST00000225275.3:c.1458G>C	ENSP00000225275.3:p.Val486=
NM_000250.1:c.1458G>C , LRG_84t1:c.1458G>C	NP_000241.1:p.Val486=
XM_011524821.1:c.1644G>C	XP_011523123.1:p.Val548=
XM_011524822.1:c.1173G>C	XP_011523124.1:p.Val391=
XM_011524823.1:c.*7G>C	XP_011523125.1:n.*7G>C
NM_000250.2:c.1458G>C MANE Select	NP_000241.1:p.Val486=