Canonical Allele Identifier: CA501022868

Gene: MPO

Linked Data

• MyVariant Identifiers: chr17:g.56350917G>C (hg19)

Genomic Alleles

HGVS	Genome Assembly
NC_000017.11:g.58273556G>C , CM000679.2:g.58273556G>C	GRCh38
NC_000017.10:g.56350917G>C , CM000679.1:g.56350917G>C	GRCh37
NC_000017.9:g.53705916G>C	NCBI36
NG_009629.1:g.12380C>G , LRG_84:g.12380C>G

Transcript Alleles

HGVS	Amino-acid Change
ENST00000578493.2:n.812C>G
ENST00000699291.1:c.604C>G	ENSP00000514272.1:n.604C>G
ENST00000699292.1:n.519C>G
ENST00000225275.4:c.1479C>G MANE Select	ENSP00000225275.3:p.Val493=
ENST00000225275.3:c.1479C>G	ENSP00000225275.3:p.Val493=
NM_000250.1:c.1479C>G , LRG_84t1:c.1479C>G	NP_000241.1:p.Val493=
XM_011524821.1:c.1665C>G	XP_011523123.1:p.Val555=
XM_011524822.1:c.1194C>G	XP_011523124.1:p.Val398=
XM_011524823.1:c.*28C>G	XP_011523125.1:n.*28C>G
NM_000250.2:c.1479C>G MANE Select	NP_000241.1:p.Val493=