Canonical Allele Identifier: CA2638971644

Gene: MPO

Linked Data

• gnomAD v4: 17-58273377-T-C

Genomic Alleles

HGVS	Genome Assembly
NC_000017.11:g.58273377T>C , CM000679.2:g.58273377T>C	GRCh38
NC_000017.10:g.56350738T>C , CM000679.1:g.56350738T>C	GRCh37
NC_000017.9:g.53705737T>C	NCBI36
NG_009629.1:g.12559A>G , LRG_84:g.12559A>G

Transcript Alleles

HGVS	Amino-acid change
ENST00000578493.2:n.954+37A>G
ENST00000699291.1:c.746+37A>G	ENSP00000514272.1:n.746+37A>G
ENST00000699292.1:n.698A>G
ENST00000225275.4:c.1621+37A>G MANE Select	ENSP00000225275.3:n.1621+37A>G
ENST00000225275.3:c.1621+37A>G	ENSP00000225275.3:n.1621+37A>G
ENST00000577220.1:c.79+37A>G	ENSP00000464668.1:n.79+37A>G
NM_000250.1:c.1621+37A>G , LRG_84t1:c.1621+37A>G	NP_000241.1:n.1621+37A>G
XM_011524821.1:c.1807+37A>G	XP_011523123.1:n.1807+37A>G
XM_011524822.1:c.1336+37A>G	XP_011523124.1:n.1336+37A>G
NM_000250.2:c.1621+37A>G MANE Select	NP_000241.1:n.1621+37A>G