Canonical Allele Identifier: CA2638971253

Gene: MPO

Linked Data

• gnomAD v4: 17-58272660-G-C

Genomic Alleles

HGVS	Genome Assembly
NC_000017.11:g.58272660G>C , CM000679.2:g.58272660G>C	GRCh38
NC_000017.10:g.56350021G>C , CM000679.1:g.56350021G>C	GRCh37
NC_000017.9:g.53705020G>C	NCBI36
NG_009629.1:g.13276C>G , LRG_84:g.13276C>G

Transcript Alleles

HGVS	Amino-acid Change
ENST00000578493.2:n.1125+88C>G
ENST00000699291.1:c.917+88C>G	ENSP00000514272.1:n.917+88C>G
ENST00000699292.1:n.1327+88C>G
ENST00000225275.4:c.1792+88C>G MANE Select	ENSP00000225275.3:n.1792+88C>G
ENST00000225275.3:c.1792+88C>G	ENSP00000225275.3:n.1792+88C>G
ENST00000577220.1:c.183+155C>G	ENSP00000464668.1:n.183+155C>G
NM_000250.1:c.1792+88C>G , LRG_84t1:c.1792+88C>G	NP_000241.1:n.1792+88C>G
XM_011524821.1:c.1978+88C>G	XP_011523123.1:n.1978+88C>G
XM_011524822.1:c.1507+88C>G	XP_011523124.1:n.1507+88C>G
NM_000250.2:c.1792+88C>G MANE Select	NP_000241.1:n.1792+88C>G