Canonical Allele Identifier: CA400370060
Gene: MPO HGNC NCBI

Linked Data

Genomic Alleles

HGVS Genome Assembly
NC_000017.11:g.58273524A>C , CM000679.2:g.58273524A>C GRCh38
NC_000017.10:g.56350885A>C , CM000679.1:g.56350885A>C GRCh37
NC_000017.9:g.53705884A>C NCBI36
NG_009629.1:g.12412T>G , LRG_84:g.12412T>G

Transcript Alleles

HGVS Amino-acid Change
ENST00000578493.2:n.844T>G
ENST00000699291.1:c.636T>G ENSP00000514272.1:n.636T>G
ENST00000699292.1:n.551T>G
ENST00000225275.4:c.1511T>G MANE Select ENSP00000225275.3:p.Leu504Arg
ENST00000225275.3:c.1511T>G ENSP00000225275.3:p.Leu504Arg
NM_000250.1:c.1511T>G , LRG_84t1:c.1511T>G NP_000241.1:p.Leu504Arg
XM_011524821.1:c.1697T>G XP_011523123.1:p.Leu566Arg
XM_011524822.1:c.1226T>G XP_011523124.1:p.Leu409Arg
XM_011524823.1:c.*60T>G XP_011523125.1:n.*60T>G
NM_000250.2:c.1511T>G MANE Select NP_000241.1:p.Leu504Arg