Canonical Allele Identifier: CA400376820

Gene: MPO

Linked Data

• MyVariant Identifiers: chr17:g.56357751T>A (hg19) ; chr17:g.58280390T>A (hg38)

Genomic Alleles

HGVS	Genome Assembly
NC_000017.11:g.58280390T>A , CM000679.2:g.58280390T>A	GRCh38
NC_000017.10:g.56357751T>A , CM000679.1:g.56357751T>A	GRCh37
NC_000017.9:g.53712750T>A	NCBI36
NG_009629.1:g.5546A>T , LRG_84:g.5546A>T

Transcript Alleles

HGVS	Amino-acid Change
ENST00000225275.4:c.224A>T MANE Select	ENSP00000225275.3:p.Lys75Met
ENST00000225275.3:c.224A>T	ENSP00000225275.3:p.Lys75Met
ENST00000580005.1:n.153A>T
NM_000250.1:c.224A>T , LRG_84t1:c.224A>T	NP_000241.1:p.Lys75Met
XM_011524821.1:c.410A>T	XP_011523123.1:p.Lys137Met
XM_011524822.1:c.-38+215A>T	XP_011523124.1:n.-38+215A>T
XM_011524823.1:c.410A>T	XP_011523125.1:p.Lys137Met
NM_000250.2:c.224A>T MANE Select	NP_000241.1:p.Lys75Met