Canonical Allele Identifier: CA400368958

Gene: MPO

Linked Data

• MyVariant Identifiers: chr17:g.56350108C>A (hg19) ; chr17:g.58272747C>A (hg38)

Genomic Alleles

HGVS	Genome Assembly
NC_000017.11:g.58272747C>A , CM000679.2:g.58272747C>A	GRCh38
NC_000017.10:g.56350108C>A , CM000679.1:g.56350108C>A	GRCh37
NC_000017.9:g.53705107C>A	NCBI36
NG_009629.1:g.13189G>T , LRG_84:g.13189G>T

Transcript Alleles

HGVS	Amino-acid change
ENST00000578493.2:n.1125+1G>T
ENST00000699291.1:c.917+1G>T	ENSP00000514272.1:n.917+1G>T
ENST00000699292.1:n.1327+1G>T
ENST00000225275.4:c.1792+1G>T MANE Select	ENSP00000225275.3:n.1792+1G>T
ENST00000225275.3:c.1792+1G>T	ENSP00000225275.3:n.1792+1G>T
ENST00000577220.1:c.183+68G>T	ENSP00000464668.1:n.183+68G>T
NM_000250.1:c.1792+1G>T , LRG_84t1:c.1792+1G>T	NP_000241.1:n.1792+1G>T
XM_011524821.1:c.1978+1G>T	XP_011523123.1:n.1978+1G>T
XM_011524822.1:c.1507+1G>T	XP_011523124.1:n.1507+1G>T
NM_000250.2:c.1792+1G>T MANE Select	NP_000241.1:n.1792+1G>T