Canonical Allele Identifier: CA501023087

Gene: MPO

Linked Data

• MyVariant Identifiers: chr17:g.56350965G>C (hg19)

Genomic Alleles

HGVS	Genome Assembly
NC_000017.11:g.58273604G>C , CM000679.2:g.58273604G>C	GRCh38
NC_000017.10:g.56350965G>C , CM000679.1:g.56350965G>C	GRCh37
NC_000017.9:g.53705964G>C	NCBI36
NG_009629.1:g.12332C>G , LRG_84:g.12332C>G

Transcript Alleles

HGVS	Amino-acid Change
ENST00000578493.2:n.764C>G
ENST00000699291.1:c.556C>G	ENSP00000514272.1:p.His186Asp
ENST00000699292.1:n.471C>G
ENST00000225275.4:c.1431C>G MANE Select	ENSP00000225275.3:p.Pro477=
ENST00000225275.3:c.1431C>G	ENSP00000225275.3:p.Pro477=
NM_000250.1:c.1431C>G , LRG_84t1:c.1431C>G	NP_000241.1:p.Pro477=
XM_011524821.1:c.1617C>G	XP_011523123.1:p.Pro539=
XM_011524822.1:c.1146C>G	XP_011523124.1:p.Pro382=
XM_011524823.1:c.1456C>G	XP_011523125.1:p.His486Asp
NM_000250.2:c.1431C>G MANE Select	NP_000241.1:p.Pro477=