Canonical Allele Identifier: CA2638971655

Gene: MPO

Linked Data

• gnomAD v4: 17-58273393-C-A

Genomic Alleles

HGVS	Genome Assembly
NC_000017.11:g.58273393C>A , CM000679.2:g.58273393C>A	GRCh38
NC_000017.10:g.56350754C>A , CM000679.1:g.56350754C>A	GRCh37
NC_000017.9:g.53705753C>A	NCBI36
NG_009629.1:g.12543G>T , LRG_84:g.12543G>T

Transcript Alleles

HGVS	Amino-acid change
ENST00000578493.2:n.954+21G>T
ENST00000699291.1:c.746+21G>T	ENSP00000514272.1:n.746+21G>T
ENST00000699292.1:n.682G>T
ENST00000225275.4:c.1621+21G>T MANE Select	ENSP00000225275.3:n.1621+21G>T
ENST00000225275.3:c.1621+21G>T	ENSP00000225275.3:n.1621+21G>T
ENST00000577220.1:c.79+21G>T	ENSP00000464668.1:n.79+21G>T
NM_000250.1:c.1621+21G>T , LRG_84t1:c.1621+21G>T	NP_000241.1:n.1621+21G>T
XM_011524821.1:c.1807+21G>T	XP_011523123.1:n.1807+21G>T
XM_011524822.1:c.1336+21G>T	XP_011523124.1:n.1336+21G>T
NM_000250.2:c.1621+21G>T MANE Select	NP_000241.1:n.1621+21G>T