Canonical Allele Identifier: CA400376831

Gene: MPO

Linked Data

• MyVariant Identifiers: chr17:g.56357754T>A (hg19) ; chr17:g.58280393T>A (hg38)

Genomic Alleles

HGVS	Genome Assembly
NC_000017.11:g.58280393T>A , CM000679.2:g.58280393T>A	GRCh38
NC_000017.10:g.56357754T>A , CM000679.1:g.56357754T>A	GRCh37
NC_000017.9:g.53712753T>A	NCBI36
NG_009629.1:g.5543A>T , LRG_84:g.5543A>T

Transcript Alleles

HGVS	Amino-acid Change
ENST00000225275.4:c.221A>T MANE Select	ENSP00000225275.3:p.Asp74Val
ENST00000225275.3:c.221A>T	ENSP00000225275.3:p.Asp74Val
ENST00000580005.1:n.150A>T
NM_000250.1:c.221A>T , LRG_84t1:c.221A>T	NP_000241.1:p.Asp74Val
XM_011524821.1:c.407A>T	XP_011523123.1:p.Asp136Val
XM_011524822.1:c.-38+212A>T	XP_011523124.1:n.-38+212A>T
XM_011524823.1:c.407A>T	XP_011523125.1:p.Asp136Val
NM_000250.2:c.221A>T MANE Select	NP_000241.1:p.Asp74Val