Canonical Allele Identifier: CA501023691

Gene: MPO

Linked Data

• MyVariant Identifiers: chr17:g.56351022A>C (hg19)

Genomic Alleles

HGVS	Genome Assembly
NC_000017.11:g.58273661A>C , CM000679.2:g.58273661A>C	GRCh38
NC_000017.10:g.56351022A>C , CM000679.1:g.56351022A>C	GRCh37
NC_000017.9:g.53706021A>C	NCBI36
NG_009629.1:g.12275T>G , LRG_84:g.12275T>G

Transcript Alleles

HGVS	Amino-acid Change
ENST00000578493.2:n.707T>G
ENST00000699291.1:c.499T>G	ENSP00000514272.1:p.Leu167Val
ENST00000699292.1:n.414T>G
ENST00000225275.4:c.1374T>G MANE Select	ENSP00000225275.3:p.Thr458=
ENST00000225275.3:c.1374T>G	ENSP00000225275.3:p.Thr458=
NM_000250.1:c.1374T>G , LRG_84t1:c.1374T>G	NP_000241.1:p.Thr458=
XM_011524821.1:c.1560T>G	XP_011523123.1:p.Thr520=
XM_011524822.1:c.1089T>G	XP_011523124.1:p.Thr363=
XM_011524823.1:c.1399T>G	XP_011523125.1:p.Leu467Val
NM_000250.2:c.1374T>G MANE Select	NP_000241.1:p.Thr458=