Canonical Allele Identifier: CA8670581

Gene: MPO

Linked Data

• dbSNP Id: rs755936324
• ExAC: 17:56350739 G / C
• gnomAD v2: 17-56350739-G-C
• gnomAD v3: 17-58273378-G-C
• gnomAD v4: 17-58273378-G-C
• COSMIC: COSN9223052
• MyVariant Identifiers: chr17:g.56350739G>C (hg19) ; chr17:g.58273378G>C (hg38)

Genomic Alleles

HGVS	Genome Assembly
NC_000017.11:g.58273378G>C , CM000679.2:g.58273378G>C	GRCh38
NC_000017.10:g.56350739G>C , CM000679.1:g.56350739G>C	GRCh37
NC_000017.9:g.53705738G>C	NCBI36
NG_009629.1:g.12558C>G , LRG_84:g.12558C>G

Transcript Alleles

HGVS	Amino-acid change
ENST00000578493.2:n.954+36C>G
ENST00000699291.1:c.746+36C>G	ENSP00000514272.1:n.746+36C>G
ENST00000699292.1:n.697C>G
ENST00000225275.4:c.1621+36C>G MANE Select	ENSP00000225275.3:n.1621+36C>G
ENST00000225275.3:c.1621+36C>G	ENSP00000225275.3:n.1621+36C>G
ENST00000577220.1:c.79+36C>G	ENSP00000464668.1:n.79+36C>G
NM_000250.1:c.1621+36C>G , LRG_84t1:c.1621+36C>G	NP_000241.1:n.1621+36C>G
XM_011524821.1:c.1807+36C>G	XP_011523123.1:n.1807+36C>G
XM_011524822.1:c.1336+36C>G	XP_011523124.1:n.1336+36C>G
NM_000250.2:c.1621+36C>G MANE Select	NP_000241.1:n.1621+36C>G