Canonical Allele Identifier: CA2638975866

Gene: MPO

Linked Data

• gnomAD v4: 17-58280910-A-C

Genomic Alleles

HGVS	Genome Assembly
NC_000017.11:g.58280910A>C , CM000679.2:g.58280910A>C	GRCh38
NC_000017.10:g.56358271A>C , CM000679.1:g.56358271A>C	GRCh37
NC_000017.9:g.53713270A>C	NCBI36
NG_009629.1:g.5026T>G , LRG_84:g.5026T>G

Transcript Alleles

HGVS	Amino-acid Change
ENST00000225275.4:c.-152T>G MANE Select	ENSP00000225275.3:n.-152T>G
ENST00000225275.3:c.-152T>G	ENSP00000225275.3:n.-152T>G
NM_000250.1:c.-152T>G , LRG_84t1:c.-152T>G	NP_000241.1:n.-152T>G
XM_011524821.1:c.215+15T>G	XP_011523123.1:n.215+15T>G
XM_011524823.1:c.215+15T>G	XP_011523125.1:n.215+15T>G
NM_000250.2:c.-152T>G MANE Select	NP_000241.1:n.-152T>G