Canonical Allele Identifier: CA400369598

Gene: MPO

Linked Data

• MyVariant Identifiers: chr17:g.56350776T>G (hg19) ; chr17:g.58273415T>G (hg38)

Genomic Alleles

HGVS	Genome Assembly
NC_000017.11:g.58273415T>G , CM000679.2:g.58273415T>G	GRCh38
NC_000017.10:g.56350776T>G , CM000679.1:g.56350776T>G	GRCh37
NC_000017.9:g.53705775T>G	NCBI36
NG_009629.1:g.12521A>C , LRG_84:g.12521A>C

Transcript Alleles

HGVS	Amino-acid change
ENST00000578493.2:n.953A>C
ENST00000699291.1:c.745A>C	ENSP00000514272.1:n.745A>C
ENST00000699292.1:n.660A>C
ENST00000225275.4:c.1620A>C MANE Select	ENSP00000225275.3:p.Glu540Asp
ENST00000225275.3:c.1620A>C	ENSP00000225275.3:p.Glu540Asp
ENST00000577220.1:c.78A>C	ENSP00000464668.1:p.Glu26Asp
NM_000250.1:c.1620A>C , LRG_84t1:c.1620A>C	NP_000241.1:p.Glu540Asp
XM_011524821.1:c.1806A>C	XP_011523123.1:p.Glu602Asp
XM_011524822.1:c.1335A>C	XP_011523124.1:p.Glu445Asp
NM_000250.2:c.1620A>C MANE Select	NP_000241.1:p.Glu540Asp