Canonical Allele Identifier: CA400369337

Gene: MPO

Linked Data

• gnomAD v4: 17-58272851-A-C
• MyVariant Identifiers: chr17:g.56350212A>C (hg19) ; chr17:g.58272851A>C (hg38)

Genomic Alleles

HGVS	Genome Assembly
NC_000017.11:g.58272851A>C , CM000679.2:g.58272851A>C	GRCh38
NC_000017.10:g.56350212A>C , CM000679.1:g.56350212A>C	GRCh37
NC_000017.9:g.53705211A>C	NCBI36
NG_009629.1:g.13085T>G , LRG_84:g.13085T>G

Transcript Alleles

HGVS	Amino-acid Change
ENST00000578493.2:n.1022T>G
ENST00000699291.1:c.814T>G	ENSP00000514272.1:n.814T>G
ENST00000699292.1:n.1224T>G
ENST00000225275.4:c.1689T>G MANE Select	ENSP00000225275.3:p.Ile563Met
ENST00000225275.3:c.1689T>G	ENSP00000225275.3:p.Ile563Met
ENST00000577220.1:c.147T>G	ENSP00000464668.1:p.Ile49Met
NM_000250.1:c.1689T>G , LRG_84t1:c.1689T>G	NP_000241.1:p.Ile563Met
XM_011524821.1:c.1875T>G	XP_011523123.1:p.Ile625Met
XM_011524822.1:c.1404T>G	XP_011523124.1:p.Ile468Met
NM_000250.2:c.1689T>G MANE Select	NP_000241.1:p.Ile563Met