Canonical Allele Identifier: CA400370148

Gene: MPO

Linked Data

• MyVariant Identifiers: chr17:g.56350903A>C (hg19) ; chr17:g.58273542A>C (hg38)

Genomic Alleles

HGVS	Genome Assembly
NC_000017.11:g.58273542A>C , CM000679.2:g.58273542A>C	GRCh38
NC_000017.10:g.56350903A>C , CM000679.1:g.56350903A>C	GRCh37
NC_000017.9:g.53705902A>C	NCBI36
NG_009629.1:g.12394T>G , LRG_84:g.12394T>G

Transcript Alleles

HGVS	Amino-acid Change
ENST00000578493.2:n.826T>G
ENST00000699291.1:c.618T>G	ENSP00000514272.1:n.618T>G
ENST00000699292.1:n.533T>G
ENST00000225275.4:c.1493T>G MANE Select	ENSP00000225275.3:p.Phe498Cys
ENST00000225275.3:c.1493T>G	ENSP00000225275.3:p.Phe498Cys
NM_000250.1:c.1493T>G , LRG_84t1:c.1493T>G	NP_000241.1:p.Phe498Cys
XM_011524821.1:c.1679T>G	XP_011523123.1:p.Phe560Cys
XM_011524822.1:c.1208T>G	XP_011523124.1:p.Phe403Cys
XM_011524823.1:c.*42T>G	XP_011523125.1:n.*42T>G
NM_000250.2:c.1493T>G MANE Select	NP_000241.1:p.Phe498Cys