Canonical Allele Identifier: CA400370146

Gene: MPO

Linked Data

• MyVariant Identifiers: chr17:g.56350902G>C (hg19) ; chr17:g.58273541G>C (hg38)

Genomic Alleles

HGVS	Genome Assembly
NC_000017.11:g.58273541G>C , CM000679.2:g.58273541G>C	GRCh38
NC_000017.10:g.56350902G>C , CM000679.1:g.56350902G>C	GRCh37
NC_000017.9:g.53705901G>C	NCBI36
NG_009629.1:g.12395C>G , LRG_84:g.12395C>G

Transcript Alleles

HGVS	Amino-acid Change
ENST00000578493.2:n.827C>G
ENST00000699291.1:c.619C>G	ENSP00000514272.1:n.619C>G
ENST00000699292.1:n.534C>G
ENST00000225275.4:c.1494C>G MANE Select	ENSP00000225275.3:p.Phe498Leu
ENST00000225275.3:c.1494C>G	ENSP00000225275.3:p.Phe498Leu
NM_000250.1:c.1494C>G , LRG_84t1:c.1494C>G	NP_000241.1:p.Phe498Leu
XM_011524821.1:c.1680C>G	XP_011523123.1:p.Phe560Leu
XM_011524822.1:c.1209C>G	XP_011523124.1:p.Phe403Leu
XM_011524823.1:c.*43C>G	XP_011523125.1:n.*43C>G
NM_000250.2:c.1494C>G MANE Select	NP_000241.1:p.Phe498Leu