Canonical Allele Identifier: CA2638971277

Gene: MPO

Linked Data

• gnomAD v4: 17-58272672-G-T

Genomic Alleles

HGVS	Genome Assembly
NC_000017.11:g.58272672G>T , CM000679.2:g.58272672G>T	GRCh38
NC_000017.10:g.56350033G>T , CM000679.1:g.56350033G>T	GRCh37
NC_000017.9:g.53705032G>T	NCBI36
NG_009629.1:g.13264C>A , LRG_84:g.13264C>A

Transcript Alleles

HGVS	Amino-acid Change
ENST00000578493.2:n.1125+76C>A
ENST00000699291.1:c.917+76C>A	ENSP00000514272.1:n.917+76C>A
ENST00000699292.1:n.1327+76C>A
ENST00000225275.4:c.1792+76C>A MANE Select	ENSP00000225275.3:n.1792+76C>A
ENST00000225275.3:c.1792+76C>A	ENSP00000225275.3:n.1792+76C>A
ENST00000577220.1:c.183+143C>A	ENSP00000464668.1:n.183+143C>A
NM_000250.1:c.1792+76C>A , LRG_84t1:c.1792+76C>A	NP_000241.1:n.1792+76C>A
XM_011524821.1:c.1978+76C>A	XP_011523123.1:n.1978+76C>A
XM_011524822.1:c.1507+76C>A	XP_011523124.1:n.1507+76C>A
NM_000250.2:c.1792+76C>A MANE Select	NP_000241.1:n.1792+76C>A