Canonical Allele Identifier: CA400370326

Gene: MPO

Linked Data

• gnomAD v4: 17-58273594-A-C
• MyVariant Identifiers: chr17:g.56350955A>C (hg19) ; chr17:g.58273594A>C (hg38)

Genomic Alleles

HGVS	Genome Assembly
NC_000017.11:g.58273594A>C , CM000679.2:g.58273594A>C	GRCh38
NC_000017.10:g.56350955A>C , CM000679.1:g.56350955A>C	GRCh37
NC_000017.9:g.53705954A>C	NCBI36
NG_009629.1:g.12342T>G , LRG_84:g.12342T>G

Transcript Alleles

HGVS	Amino-acid Change
ENST00000578493.2:n.774T>G
ENST00000699291.1:c.566T>G	ENSP00000514272.1:p.Phe189Cys
ENST00000699292.1:n.481T>G
ENST00000225275.4:c.1441T>G MANE Select	ENSP00000225275.3:p.Ser481Ala
ENST00000225275.3:c.1441T>G	ENSP00000225275.3:p.Ser481Ala
NM_000250.1:c.1441T>G , LRG_84t1:c.1441T>G	NP_000241.1:p.Ser481Ala
XM_011524821.1:c.1627T>G	XP_011523123.1:p.Ser543Ala
XM_011524822.1:c.1156T>G	XP_011523124.1:p.Ser386Ala
XM_011524823.1:c.1466T>G	XP_011523125.1:p.Phe489Cys
NM_000250.2:c.1441T>G MANE Select	NP_000241.1:p.Ser481Ala