Canonical Allele Identifier: CA292011794

Gene: MPO

Linked Data

• dbSNP Id: rs924154913
• gnomAD v2: 17-56350022-A-T
• gnomAD v3: 17-58272661-A-T
• gnomAD v4: 17-58272661-A-T
• MyVariant Identifiers: chr17:g.56350022A>T (hg19) ; chr17:g.58272661A>T (hg38)

Genomic Alleles

HGVS	Genome Assembly
NC_000017.11:g.58272661A>T , CM000679.2:g.58272661A>T	GRCh38
NC_000017.10:g.56350022A>T , CM000679.1:g.56350022A>T	GRCh37
NC_000017.9:g.53705021A>T	NCBI36
NG_009629.1:g.13275T>A , LRG_84:g.13275T>A

Transcript Alleles

HGVS	Amino-acid Change
ENST00000578493.2:n.1125+87T>A
ENST00000699291.1:c.917+87T>A	ENSP00000514272.1:n.917+87T>A
ENST00000699292.1:n.1327+87T>A
ENST00000225275.4:c.1792+87T>A MANE Select	ENSP00000225275.3:n.1792+87T>A
ENST00000225275.3:c.1792+87T>A	ENSP00000225275.3:n.1792+87T>A
ENST00000577220.1:c.183+154T>A	ENSP00000464668.1:n.183+154T>A
NM_000250.1:c.1792+87T>A , LRG_84t1:c.1792+87T>A	NP_000241.1:n.1792+87T>A
XM_011524821.1:c.1978+87T>A	XP_011523123.1:n.1978+87T>A
XM_011524822.1:c.1507+87T>A	XP_011523124.1:n.1507+87T>A
NM_000250.2:c.1792+87T>A MANE Select	NP_000241.1:n.1792+87T>A