Canonical Allele Identifier: CA8670418

Gene: MPO

Linked Data

• dbSNP Id: rs780418062
• ExAC: 17:56348134 T / C
• gnomAD v2: 17-56348134-T-C
• gnomAD v4: 17-58270773-T-C
• MyVariant Identifiers: chr17:g.56348134T>C (hg19) ; chr17:g.58270773T>C (hg38)

Genomic Alleles

HGVS	Genome Assembly
NC_000017.11:g.58270773T>C , CM000679.2:g.58270773T>C	GRCh38
NC_000017.10:g.56348134T>C , CM000679.1:g.56348134T>C	GRCh37
NC_000017.9:g.53703133T>C	NCBI36
NG_009629.1:g.15163A>G , LRG_84:g.15163A>G

Transcript Alleles

HGVS	Amino-acid change
ENST00000578493.2:n.1454A>G
ENST00000699291.1:c.1246A>G	ENSP00000514272.1:n.1246A>G
ENST00000699292.1:n.1656A>G
ENST00000225275.4:c.2121A>G MANE Select	ENSP00000225275.3:p.Thr707=
ENST00000225275.3:c.2121A>G	ENSP00000225275.3:p.Thr707=
ENST00000577220.1:c.216A>G	ENSP00000464668.1:p.Thr72=
NM_000250.1:c.2121A>G , LRG_84t1:c.2121A>G	NP_000241.1:p.Thr707=
XM_011524821.1:c.2307A>G	XP_011523123.1:p.Thr769=
XM_011524822.1:c.1836A>G	XP_011523124.1:p.Thr612=
NM_000250.2:c.2121A>G MANE Select	NP_000241.1:p.Thr707=