Canonical Allele Identifier: CA2638975872

Gene: MPO

Linked Data

• gnomAD v4: 17-58280914-C-A

Genomic Alleles

HGVS	Genome Assembly
NC_000017.11:g.58280914C>A , CM000679.2:g.58280914C>A	GRCh38
NC_000017.10:g.56358275C>A , CM000679.1:g.56358275C>A	GRCh37
NC_000017.9:g.53713274C>A	NCBI36
NG_009629.1:g.5022G>T , LRG_84:g.5022G>T

Transcript Alleles

HGVS	Amino-acid Change
ENST00000225275.4:c.-156G>T MANE Select	ENSP00000225275.3:n.-156G>T
ENST00000225275.3:c.-156G>T	ENSP00000225275.3:n.-156G>T
NM_000250.1:c.-156G>T , LRG_84t1:c.-156G>T	NP_000241.1:n.-156G>T
XM_011524821.1:c.215+11G>T	XP_011523123.1:n.215+11G>T
XM_011524823.1:c.215+11G>T	XP_011523125.1:n.215+11G>T
NM_000250.2:c.-156G>T MANE Select	NP_000241.1:n.-156G>T