Canonical Allele Identifier: CA400370525

Gene: MPO

Linked Data

• dbSNP Id: rs1360305844
• gnomAD v4: 17-58273654-C-T
• MyVariant Identifiers: chr17:g.56351015C>T (hg19) ; chr17:g.58273654C>T (hg38)

Genomic Alleles

HGVS	Genome Assembly
NC_000017.11:g.58273654C>T , CM000679.2:g.58273654C>T	GRCh38
NC_000017.10:g.56351015C>T , CM000679.1:g.56351015C>T	GRCh37
NC_000017.9:g.53706014C>T	NCBI36
NG_009629.1:g.12282G>A , LRG_84:g.12282G>A

Transcript Alleles

HGVS	Amino-acid Change
ENST00000578493.2:n.714G>A
ENST00000699291.1:c.506G>A	ENSP00000514272.1:p.Gly169Glu
ENST00000699292.1:n.421G>A
ENST00000225275.4:c.1381G>A MANE Select	ENSP00000225275.3:p.Asp461Asn
ENST00000225275.3:c.1381G>A	ENSP00000225275.3:p.Asp461Asn
NM_000250.1:c.1381G>A , LRG_84t1:c.1381G>A	NP_000241.1:p.Asp461Asn
XM_011524821.1:c.1567G>A	XP_011523123.1:p.Asp523Asn
XM_011524822.1:c.1096G>A	XP_011523124.1:p.Asp366Asn
XM_011524823.1:c.1406G>A	XP_011523125.1:p.Gly469Glu
NM_000250.2:c.1381G>A MANE Select	NP_000241.1:p.Asp461Asn