Canonical Allele Identifier: CA400370387

Gene: MPO

Linked Data

• MyVariant Identifiers: chr17:g.56350973A>T (hg19) ; chr17:g.58273612A>T (hg38)

Genomic Alleles

HGVS	Genome Assembly
NC_000017.11:g.58273612A>T , CM000679.2:g.58273612A>T	GRCh38
NC_000017.10:g.56350973A>T , CM000679.1:g.56350973A>T	GRCh37
NC_000017.9:g.53705972A>T	NCBI36
NG_009629.1:g.12324T>A , LRG_84:g.12324T>A

Transcript Alleles

HGVS	Amino-acid Change
ENST00000578493.2:n.756T>A
ENST00000699291.1:c.548T>A	ENSP00000514272.1:p.Val183Glu
ENST00000699292.1:n.463T>A
ENST00000225275.4:c.1423T>A MANE Select	ENSP00000225275.3:p.Tyr475Asn
ENST00000225275.3:c.1423T>A	ENSP00000225275.3:p.Tyr475Asn
NM_000250.1:c.1423T>A , LRG_84t1:c.1423T>A	NP_000241.1:p.Tyr475Asn
XM_011524821.1:c.1609T>A	XP_011523123.1:p.Tyr537Asn
XM_011524822.1:c.1138T>A	XP_011523124.1:p.Tyr380Asn
XM_011524823.1:c.1448T>A	XP_011523125.1:p.Val483Glu
NM_000250.2:c.1423T>A MANE Select	NP_000241.1:p.Tyr475Asn