Canonical Allele Identifier: CA400370354

Gene: MPO

Linked Data

• COSMIC: COSM4451845 ; COSM4451846
• MyVariant Identifiers: chr17:g.56350964T>A (hg19) ; chr17:g.58273603T>A (hg38)

Genomic Alleles

HGVS	Genome Assembly
NC_000017.11:g.58273603T>A , CM000679.2:g.58273603T>A	GRCh38
NC_000017.10:g.56350964T>A , CM000679.1:g.56350964T>A	GRCh37
NC_000017.9:g.53705963T>A	NCBI36
NG_009629.1:g.12333A>T , LRG_84:g.12333A>T

Transcript Alleles

HGVS	Amino-acid Change
ENST00000578493.2:n.765A>T
ENST00000699291.1:c.557A>T	ENSP00000514272.1:p.His186Leu
ENST00000699292.1:n.472A>T
ENST00000225275.4:c.1432A>T MANE Select	ENSP00000225275.3:p.Thr478Ser
ENST00000225275.3:c.1432A>T	ENSP00000225275.3:p.Thr478Ser
NM_000250.1:c.1432A>T , LRG_84t1:c.1432A>T	NP_000241.1:p.Thr478Ser
XM_011524821.1:c.1618A>T	XP_011523123.1:p.Thr540Ser
XM_011524822.1:c.1147A>T	XP_011523124.1:p.Thr383Ser
XM_011524823.1:c.1457A>T	XP_011523125.1:p.His486Leu
NM_000250.2:c.1432A>T MANE Select	NP_000241.1:p.Thr478Ser