Canonical Allele Identifier: CA400369769

Gene: MPO

Linked Data

• MyVariant Identifiers: chr17:g.56350814T>A (hg19) ; chr17:g.58273453T>A (hg38)

Genomic Alleles

HGVS	Genome Assembly
NC_000017.11:g.58273453T>A , CM000679.2:g.58273453T>A	GRCh38
NC_000017.10:g.56350814T>A , CM000679.1:g.56350814T>A	GRCh37
NC_000017.9:g.53705813T>A	NCBI36
NG_009629.1:g.12483A>T , LRG_84:g.12483A>T

Transcript Alleles

HGVS	Amino-acid Change
ENST00000578493.2:n.915A>T
ENST00000699291.1:c.707A>T	ENSP00000514272.1:n.707A>T
ENST00000699292.1:n.622A>T
ENST00000225275.4:c.1582A>T MANE Select	ENSP00000225275.3:p.Ser528Cys
ENST00000225275.3:c.1582A>T	ENSP00000225275.3:p.Ser528Cys
ENST00000577220.1:c.40A>T	ENSP00000464668.1:p.Ser14Cys
NM_000250.1:c.1582A>T , LRG_84t1:c.1582A>T	NP_000241.1:p.Ser528Cys
XM_011524821.1:c.1768A>T	XP_011523123.1:p.Ser590Cys
XM_011524822.1:c.1297A>T	XP_011523124.1:p.Ser433Cys
XM_011524823.1:c.*131A>T	XP_011523125.1:n.*131A>T
NM_000250.2:c.1582A>T MANE Select	NP_000241.1:p.Ser528Cys