Canonical Allele Identifier: CA400376823
Gene: MPO HGNC NCBI

Linked Data

MyVariant Identifiers: chr17:g.56357752T>C (hg19) chr17:g.58280391T>C (hg38)
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Genomic Alleles

HGVS Genome Assembly
NC_000017.11:g.58280391T>C , CM000679.2:g.58280391T>C GRCh38
NC_000017.10:g.56357752T>C , CM000679.1:g.56357752T>C GRCh37
NC_000017.9:g.53712751T>C NCBI36
NG_009629.1:g.5545A>G , LRG_84:g.5545A>G

Transcript Alleles

HGVS Amino-acid change
ENST00000225275.4:c.223A>G MANE Select ENSP00000225275.3:p.Lys75Glu
ENST00000225275.3:c.223A>G ENSP00000225275.3:p.Lys75Glu
ENST00000580005.1:n.152A>G
NM_000250.1:c.223A>G , LRG_84t1:c.223A>G NP_000241.1:p.Lys75Glu
XM_011524821.1:c.409A>G XP_011523123.1:p.Lys137Glu
XM_011524822.1:c.-38+214A>G XP_011523124.1:n.-38+214A>G
XM_011524823.1:c.409A>G XP_011523125.1:p.Lys137Glu
NM_000250.2:c.223A>G MANE Select NP_000241.1:p.Lys75Glu
Search 100 bp 5'
Search 100 bp 3'