Canonical Allele Identifier: CA400370523

Gene: MPO

Linked Data

• MyVariant Identifiers: chr17:g.56351015C>A (hg19) ; chr17:g.58273654C>A (hg38)

Genomic Alleles

HGVS	Genome Assembly
NC_000017.11:g.58273654C>A , CM000679.2:g.58273654C>A	GRCh38
NC_000017.10:g.56351015C>A , CM000679.1:g.56351015C>A	GRCh37
NC_000017.9:g.53706014C>A	NCBI36
NG_009629.1:g.12282G>T , LRG_84:g.12282G>T

Transcript Alleles

HGVS	Amino-acid Change
ENST00000578493.2:n.714G>T
ENST00000699291.1:c.506G>T	ENSP00000514272.1:p.Gly169Val
ENST00000699292.1:n.421G>T
ENST00000225275.4:c.1381G>T MANE Select	ENSP00000225275.3:p.Asp461Tyr
ENST00000225275.3:c.1381G>T	ENSP00000225275.3:p.Asp461Tyr
NM_000250.1:c.1381G>T , LRG_84t1:c.1381G>T	NP_000241.1:p.Asp461Tyr
XM_011524821.1:c.1567G>T	XP_011523123.1:p.Asp523Tyr
XM_011524822.1:c.1096G>T	XP_011523124.1:p.Asp366Tyr
XM_011524823.1:c.1406G>T	XP_011523125.1:p.Gly469Val
NM_000250.2:c.1381G>T MANE Select	NP_000241.1:p.Asp461Tyr