Canonical Allele Identifier: CA400368984

Gene: MPO

Linked Data

• MyVariant Identifiers: chr17:g.56350120T>G (hg19) ; chr17:g.58272759T>G (hg38)

Genomic Alleles

HGVS	Genome Assembly
NC_000017.11:g.58272759T>G , CM000679.2:g.58272759T>G	GRCh38
NC_000017.10:g.56350120T>G , CM000679.1:g.56350120T>G	GRCh37
NC_000017.9:g.53705119T>G	NCBI36
NG_009629.1:g.13177A>C , LRG_84:g.13177A>C

Transcript Alleles

HGVS	Amino-acid change
ENST00000578493.2:n.1114A>C
ENST00000699291.1:c.906A>C	ENSP00000514272.1:n.906A>C
ENST00000699292.1:n.1316A>C
ENST00000225275.4:c.1781A>C MANE Select	ENSP00000225275.3:p.His594Pro
ENST00000225275.3:c.1781A>C	ENSP00000225275.3:p.His594Pro
ENST00000577220.1:c.183+56A>C	ENSP00000464668.1:n.183+56A>C
NM_000250.1:c.1781A>C , LRG_84t1:c.1781A>C	NP_000241.1:p.His594Pro
XM_011524821.1:c.1967A>C	XP_011523123.1:p.His656Pro
XM_011524822.1:c.1496A>C	XP_011523124.1:p.His499Pro
NM_000250.2:c.1781A>C MANE Select	NP_000241.1:p.His594Pro