Canonical Allele Identifier: CA400370177

Gene: MPO

Linked Data

• dbSNP Id: rs1475242192
• gnomAD v2: 17-56350910-T-C
• gnomAD v4: 17-58273549-T-C
• MyVariant Identifiers: chr17:g.56350910T>C (hg19) ; chr17:g.58273549T>C (hg38)

Genomic Alleles

HGVS	Genome Assembly
NC_000017.11:g.58273549T>C , CM000679.2:g.58273549T>C	GRCh38
NC_000017.10:g.56350910T>C , CM000679.1:g.56350910T>C	GRCh37
NC_000017.9:g.53705909T>C	NCBI36
NG_009629.1:g.12387A>G , LRG_84:g.12387A>G

Transcript Alleles

HGVS	Amino-acid Change
ENST00000578493.2:n.819A>G
ENST00000699291.1:c.611A>G	ENSP00000514272.1:n.611A>G
ENST00000699292.1:n.526A>G
ENST00000225275.4:c.1486A>G MANE Select	ENSP00000225275.3:p.Asn496Asp
ENST00000225275.3:c.1486A>G	ENSP00000225275.3:p.Asn496Asp
NM_000250.1:c.1486A>G , LRG_84t1:c.1486A>G	NP_000241.1:p.Asn496Asp
XM_011524821.1:c.1672A>G	XP_011523123.1:p.Asn558Asp
XM_011524822.1:c.1201A>G	XP_011523124.1:p.Asn401Asp
XM_011524823.1:c.*35A>G	XP_011523125.1:n.*35A>G
NM_000250.2:c.1486A>G MANE Select	NP_000241.1:p.Asn496Asp