Canonical Allele Identifier: CA292012265

Gene: MPO

Linked Data

• dbSNP Id: rs919082375
• MyVariant Identifiers: chr17:g.56350889T>C (hg19) ; chr17:g.58273528T>C (hg38)

Genomic Alleles

HGVS	Genome Assembly
NC_000017.11:g.58273528T>C , CM000679.2:g.58273528T>C	GRCh38
NC_000017.10:g.56350889T>C , CM000679.1:g.56350889T>C	GRCh37
NC_000017.9:g.53705888T>C	NCBI36
NG_009629.1:g.12408A>G , LRG_84:g.12408A>G

Transcript Alleles

HGVS	Amino-acid Change
ENST00000578493.2:n.840A>G
ENST00000699291.1:c.632A>G	ENSP00000514272.1:n.632A>G
ENST00000699292.1:n.547A>G
ENST00000225275.4:c.1507A>G MANE Select	ENSP00000225275.3:p.Thr503Ala
ENST00000225275.3:c.1507A>G	ENSP00000225275.3:p.Thr503Ala
NM_000250.1:c.1507A>G , LRG_84t1:c.1507A>G	NP_000241.1:p.Thr503Ala
XM_011524821.1:c.1693A>G	XP_011523123.1:p.Thr565Ala
XM_011524822.1:c.1222A>G	XP_011523124.1:p.Thr408Ala
XM_011524823.1:c.*56A>G	XP_011523125.1:n.*56A>G
NM_000250.2:c.1507A>G MANE Select	NP_000241.1:p.Thr503Ala