Canonical Allele Identifier: CA400370553

Gene: MPO

Linked Data

• dbSNP Id: rs1355215148
• MyVariant Identifiers: chr17:g.56351024T>C (hg19) ; chr17:g.58273663T>C (hg38)

Genomic Alleles

HGVS	Genome Assembly
NC_000017.11:g.58273663T>C , CM000679.2:g.58273663T>C	GRCh38
NC_000017.10:g.56351024T>C , CM000679.1:g.56351024T>C	GRCh37
NC_000017.9:g.53706023T>C	NCBI36
NG_009629.1:g.12273A>G , LRG_84:g.12273A>G

Transcript Alleles

HGVS	Amino-acid Change
ENST00000578493.2:n.705A>G
ENST00000699291.1:c.497A>G	ENSP00000514272.1:p.His166Arg
ENST00000699292.1:n.412A>G
ENST00000225275.4:c.1372A>G MANE Select	ENSP00000225275.3:p.Thr458Ala
ENST00000225275.3:c.1372A>G	ENSP00000225275.3:p.Thr458Ala
NM_000250.1:c.1372A>G , LRG_84t1:c.1372A>G	NP_000241.1:p.Thr458Ala
XM_011524821.1:c.1558A>G	XP_011523123.1:p.Thr520Ala
XM_011524822.1:c.1087A>G	XP_011523124.1:p.Thr363Ala
XM_011524823.1:c.1397A>G	XP_011523125.1:p.His466Arg
NM_000250.2:c.1372A>G MANE Select	NP_000241.1:p.Thr458Ala