Canonical Allele Identifier: CA400376863

Gene: MPO

Linked Data

• MyVariant Identifiers: chr17:g.56357760A>T (hg19) ; chr17:g.58280399A>T (hg38)

Genomic Alleles

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

Transcript Alleles

HGVS	Amino-acid Change
ENST00000225275.4:c.215T>A MANE Select	ENSP00000225275.3:p.Leu72Gln
ENST00000225275.3:c.215T>A	ENSP00000225275.3:p.Leu72Gln
ENST00000580005.1:n.144T>A
NM_000250.1:c.215T>A , LRG_84t1:c.215T>A	NP_000241.1:p.Leu72Gln
XM_011524821.1:c.401T>A	XP_011523123.1:p.Leu134Gln
XM_011524822.1:c.-38+206T>A	XP_011523124.1:n.-38+206T>A
XM_011524823.1:c.401T>A	XP_011523125.1:p.Leu134Gln
NM_000250.2:c.215T>A MANE Select	NP_000241.1:p.Leu72Gln