Canonical Allele Identifier: CA400376825

Gene: MPO

Linked Data

• MyVariant Identifiers: chr17:g.56357752T>G (hg19) ; chr17:g.58280391T>G (hg38)

Genomic Alleles

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

Transcript Alleles

HGVS	Amino-acid change
ENST00000225275.4:c.223A>C MANE Select	ENSP00000225275.3:p.Lys75Gln
ENST00000225275.3:c.223A>C	ENSP00000225275.3:p.Lys75Gln
ENST00000580005.1:n.152A>C
NM_000250.1:c.223A>C , LRG_84t1:c.223A>C	NP_000241.1:p.Lys75Gln
XM_011524821.1:c.409A>C	XP_011523123.1:p.Lys137Gln
XM_011524822.1:c.-38+214A>C	XP_011523124.1:n.-38+214A>C
XM_011524823.1:c.409A>C	XP_011523125.1:p.Lys137Gln
NM_000250.2:c.223A>C MANE Select	NP_000241.1:p.Lys75Gln