Canonical Allele Identifier: CA400376868
Gene: MPO HGNC NCBI

Linked Data

Genomic Alleles

HGVS Genome Assembly
NC_000017.11:g.58280399A>C , CM000679.2:g.58280399A>C GRCh38
NC_000017.10:g.56357760A>C , CM000679.1:g.56357760A>C GRCh37
NC_000017.9:g.53712759A>C NCBI36
NG_009629.1:g.5537T>G , LRG_84:g.5537T>G

Transcript Alleles

HGVS Amino-acid Change
ENST00000225275.4:c.215T>G MANE Select ENSP00000225275.3:p.Leu72Arg
ENST00000225275.3:c.215T>G ENSP00000225275.3:p.Leu72Arg
ENST00000580005.1:n.144T>G
NM_000250.1:c.215T>G , LRG_84t1:c.215T>G NP_000241.1:p.Leu72Arg
XM_011524821.1:c.401T>G XP_011523123.1:p.Leu134Arg
XM_011524822.1:c.-38+206T>G XP_011523124.1:n.-38+206T>G
XM_011524823.1:c.401T>G XP_011523125.1:p.Leu134Arg
NM_000250.2:c.215T>G MANE Select NP_000241.1:p.Leu72Arg