Canonical Allele Identifier: CA2638975887

Gene: MPO

Linked Data

• gnomAD v4: 17-58280926-T-A

Genomic Alleles

HGVS	Genome Assembly
NC_000017.11:g.58280926T>A , CM000679.2:g.58280926T>A	GRCh38
NC_000017.10:g.56358287T>A , CM000679.1:g.56358287T>A	GRCh37
NC_000017.9:g.53713286T>A	NCBI36
NG_009629.1:g.5010A>T , LRG_84:g.5010A>T

Transcript Alleles

HGVS	Amino-acid Change
ENST00000225275.4:c.-168A>T MANE Select	ENSP00000225275.3:n.-168A>T
ENST00000225275.3:c.-168A>T	ENSP00000225275.3:n.-168A>T
NM_000250.1:c.-168A>T , LRG_84t1:c.-168A>T	NP_000241.1:n.-168A>T
XM_011524821.1:c.214A>T	XP_011523123.1:p.Arg72Ter
XM_011524823.1:c.214A>T	XP_011523125.1:p.Arg72Ter
NM_000250.2:c.-168A>T MANE Select	NP_000241.1:n.-168A>T