Canonical Allele Identifier: CA400370346

Gene: MPO

Linked Data

• MyVariant Identifiers: chr17:g.56350961A>G (hg19) ; chr17:g.58273600A>G (hg38)

Genomic Alleles

HGVS	Genome Assembly
NC_000017.11:g.58273600A>G , CM000679.2:g.58273600A>G	GRCh38
NC_000017.10:g.56350961A>G , CM000679.1:g.56350961A>G	GRCh37
NC_000017.9:g.53705960A>G	NCBI36
NG_009629.1:g.12336T>C , LRG_84:g.12336T>C

Transcript Alleles

HGVS	Amino-acid Change
ENST00000578493.2:n.768T>C
ENST00000699291.1:c.560T>C	ENSP00000514272.1:p.Val187Ala
ENST00000699292.1:n.475T>C
ENST00000225275.4:c.1435T>C MANE Select	ENSP00000225275.3:p.Tyr479His
ENST00000225275.3:c.1435T>C	ENSP00000225275.3:p.Tyr479His
NM_000250.1:c.1435T>C , LRG_84t1:c.1435T>C	NP_000241.1:p.Tyr479His
XM_011524821.1:c.1621T>C	XP_011523123.1:p.Tyr541His
XM_011524822.1:c.1150T>C	XP_011523124.1:p.Tyr384His
XM_011524823.1:c.1460T>C	XP_011523125.1:p.Val487Ala
NM_000250.2:c.1435T>C MANE Select	NP_000241.1:p.Tyr479His