Canonical Allele Identifier: CA2733810782

Gene: MPO

Linked Data

• dbSNP Id: rs2143968957

Genomic Alleles

HGVS	Genome Assembly
NC_000017.11:g.58273386_58273397del , CM000679.2:g.58273386_58273397del	GRCh38
NC_000017.10:g.56350747_56350758del , CM000679.1:g.56350747_56350758del	GRCh37
NC_000017.9:g.53705746_53705757del	NCBI36
NG_009629.1:g.12539_12550del , LRG_84:g.12539_12550del

Transcript Alleles

HGVS	Amino-acid change
ENST00000578493.2:n.954+17_954+28del
ENST00000699291.1:c.746+17_746+28del	ENSP00000514272.1:n.746+17_746+28del
ENST00000699292.1:n.678_689del
ENST00000225275.4:c.1621+17_1621+28del MANE Select	ENSP00000225275.3:n.1621+17_1621+28del
ENST00000225275.3:c.1621+17_1621+28del	ENSP00000225275.3:n.1621+17_1621+28del
ENST00000577220.1:c.79+17_79+28del	ENSP00000464668.1:n.79+17_79+28del
NM_000250.1:c.1621+17_1621+28del , LRG_84t1:c.1621+17_1621+28del	NP_000241.1:n.1621+17_1621+28del
XM_011524821.1:c.1807+17_1807+28del	XP_011523123.1:n.1807+17_1807+28del
XM_011524822.1:c.1336+17_1336+28del	XP_011523124.1:n.1336+17_1336+28del
NM_000250.2:c.1621+17_1621+28del MANE Select	NP_000241.1:n.1621+17_1621+28del