Canonical Allele Identifier: CA400370356

Gene: MPO

Linked Data

• gnomAD v4: 17-58273603-T-C
• MyVariant Identifiers: chr17:g.56350964T>C (hg19) ; chr17:g.58273603T>C (hg38)

Genomic Alleles

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

Transcript Alleles

HGVS	Amino-acid Change
ENST00000578493.2:n.765A>G
ENST00000699291.1:c.557A>G	ENSP00000514272.1:p.His186Arg
ENST00000699292.1:n.472A>G
ENST00000225275.4:c.1432A>G MANE Select	ENSP00000225275.3:p.Thr478Ala
ENST00000225275.3:c.1432A>G	ENSP00000225275.3:p.Thr478Ala
NM_000250.1:c.1432A>G , LRG_84t1:c.1432A>G	NP_000241.1:p.Thr478Ala
XM_011524821.1:c.1618A>G	XP_011523123.1:p.Thr540Ala
XM_011524822.1:c.1147A>G	XP_011523124.1:p.Thr383Ala
XM_011524823.1:c.1457A>G	XP_011523125.1:p.His486Arg
NM_000250.2:c.1432A>G MANE Select	NP_000241.1:p.Thr478Ala