Canonical Allele Identifier: CA400370343

Gene: MPO

Linked Data

• MyVariant Identifiers: chr17:g.56350960T>C (hg19) ; chr17:g.58273599T>C (hg38)

Genomic Alleles

HGVS	Genome Assembly
NC_000017.11:g.58273599T>C , CM000679.2:g.58273599T>C	GRCh38
NC_000017.10:g.56350960T>C , CM000679.1:g.56350960T>C	GRCh37
NC_000017.9:g.53705959T>C	NCBI36
NG_009629.1:g.12337A>G , LRG_84:g.12337A>G

Transcript Alleles

HGVS	Amino-acid Change
ENST00000578493.2:n.769A>G
ENST00000699291.1:c.561A>G	ENSP00000514272.1:p.Val187=
ENST00000699292.1:n.476A>G
ENST00000225275.4:c.1436A>G MANE Select	ENSP00000225275.3:p.Tyr479Cys
ENST00000225275.3:c.1436A>G	ENSP00000225275.3:p.Tyr479Cys
NM_000250.1:c.1436A>G , LRG_84t1:c.1436A>G	NP_000241.1:p.Tyr479Cys
XM_011524821.1:c.1622A>G	XP_011523123.1:p.Tyr541Cys
XM_011524822.1:c.1151A>G	XP_011523124.1:p.Tyr384Cys
XM_011524823.1:c.1461A>G	XP_011523125.1:p.Val487=
NM_000250.2:c.1436A>G MANE Select	NP_000241.1:p.Tyr479Cys