Canonical Allele Identifier: CA400370481

Gene: MPO

Linked Data

• gnomAD v4: 17-58273639-C-T
• MyVariant Identifiers: chr17:g.56351000C>T (hg19) ; chr17:g.58273639C>T (hg38)

Genomic Alleles

HGVS	Genome Assembly
NC_000017.11:g.58273639C>T , CM000679.2:g.58273639C>T	GRCh38
NC_000017.10:g.56351000C>T , CM000679.1:g.56351000C>T	GRCh37
NC_000017.9:g.53705999C>T	NCBI36
NG_009629.1:g.12297G>A , LRG_84:g.12297G>A

Transcript Alleles

HGVS	Amino-acid Change
ENST00000578493.2:n.729G>A
ENST00000699291.1:c.521G>A	ENSP00000514272.1:p.Gly174Asp
ENST00000699292.1:n.436G>A
ENST00000225275.4:c.1396G>A MANE Select	ENSP00000225275.3:p.Val466Met
ENST00000225275.3:c.1396G>A	ENSP00000225275.3:p.Val466Met
NM_000250.1:c.1396G>A , LRG_84t1:c.1396G>A	NP_000241.1:p.Val466Met
XM_011524821.1:c.1582G>A	XP_011523123.1:p.Val528Met
XM_011524822.1:c.1111G>A	XP_011523124.1:p.Val371Met
XM_011524823.1:c.1421G>A	XP_011523125.1:p.Gly474Asp
NM_000250.2:c.1396G>A MANE Select	NP_000241.1:p.Val466Met