Canonical Allele Identifier: CA400369278

Gene: MPO

Linked Data

• gnomAD v4: 17-58272838-T-A
• MyVariant Identifiers: chr17:g.56350199T>A (hg19) ; chr17:g.58272838T>A (hg38)

Genomic Alleles

HGVS	Genome Assembly
NC_000017.11:g.58272838T>A , CM000679.2:g.58272838T>A	GRCh38
NC_000017.10:g.56350199T>A , CM000679.1:g.56350199T>A	GRCh37
NC_000017.9:g.53705198T>A	NCBI36
NG_009629.1:g.13098A>T , LRG_84:g.13098A>T

Transcript Alleles

HGVS	Amino-acid change
ENST00000578493.2:n.1035A>T
ENST00000699291.1:c.827A>T	ENSP00000514272.1:n.827A>T
ENST00000699292.1:n.1237A>T
ENST00000225275.4:c.1702A>T MANE Select	ENSP00000225275.3:p.Ile568Phe
ENST00000225275.3:c.1702A>T	ENSP00000225275.3:p.Ile568Phe
ENST00000577220.1:c.160A>T	ENSP00000464668.1:p.Ile54Phe
NM_000250.1:c.1702A>T , LRG_84t1:c.1702A>T	NP_000241.1:p.Ile568Phe
XM_011524821.1:c.1888A>T	XP_011523123.1:p.Ile630Phe
XM_011524822.1:c.1417A>T	XP_011523124.1:p.Ile473Phe
NM_000250.2:c.1702A>T MANE Select	NP_000241.1:p.Ile568Phe