Canonical Allele Identifier: CA400369804

Gene: MPO

Linked Data

• gnomAD v4: 17-58273462-C-A
• MyVariant Identifiers: chr17:g.56350823C>A (hg19) ; chr17:g.58273462C>A (hg38)

Genomic Alleles

HGVS	Genome Assembly
NC_000017.11:g.58273462C>A , CM000679.2:g.58273462C>A	GRCh38
NC_000017.10:g.56350823C>A , CM000679.1:g.56350823C>A	GRCh37
NC_000017.9:g.53705822C>A	NCBI36
NG_009629.1:g.12474G>T , LRG_84:g.12474G>T

Transcript Alleles

HGVS	Amino-acid Change
ENST00000578493.2:n.906G>T
ENST00000699291.1:c.698G>T	ENSP00000514272.1:n.698G>T
ENST00000699292.1:n.613G>T
ENST00000225275.4:c.1573G>T MANE Select	ENSP00000225275.3:p.Val525Phe
ENST00000225275.3:c.1573G>T	ENSP00000225275.3:p.Val525Phe
ENST00000577220.1:c.31G>T	ENSP00000464668.1:p.Val11Phe
NM_000250.1:c.1573G>T , LRG_84t1:c.1573G>T	NP_000241.1:p.Val525Phe
XM_011524821.1:c.1759G>T	XP_011523123.1:p.Val587Phe
XM_011524822.1:c.1288G>T	XP_011523124.1:p.Val430Phe
XM_011524823.1:c.*122G>T	XP_011523125.1:n.*122G>T
NM_000250.2:c.1573G>T MANE Select	NP_000241.1:p.Val525Phe