Canonical Allele Identifier: CA292012136

Gene: MPO

Linked Data

• dbSNP Id: rs746472342
• gnomAD v2: 17-56350750-C-T
• gnomAD v3: 17-58273389-C-T
• gnomAD v4: 17-58273389-C-T
• MyVariant Identifiers: chr17:g.56350750C>T (hg19) ; chr17:g.58273389C>T (hg38)

Genomic Alleles

HGVS	Genome Assembly
NC_000017.11:g.58273389C>T , CM000679.2:g.58273389C>T	GRCh38
NC_000017.10:g.56350750C>T , CM000679.1:g.56350750C>T	GRCh37
NC_000017.9:g.53705749C>T	NCBI36
NG_009629.1:g.12547G>A , LRG_84:g.12547G>A

Transcript Alleles

HGVS	Amino-acid change
ENST00000578493.2:n.954+25G>A
ENST00000699291.1:c.746+25G>A	ENSP00000514272.1:n.746+25G>A
ENST00000699292.1:n.686G>A
ENST00000225275.4:c.1621+25G>A MANE Select	ENSP00000225275.3:n.1621+25G>A
ENST00000225275.3:c.1621+25G>A	ENSP00000225275.3:n.1621+25G>A
ENST00000577220.1:c.79+25G>A	ENSP00000464668.1:n.79+25G>A
NM_000250.1:c.1621+25G>A , LRG_84t1:c.1621+25G>A	NP_000241.1:n.1621+25G>A
XM_011524821.1:c.1807+25G>A	XP_011523123.1:n.1807+25G>A
XM_011524822.1:c.1336+25G>A	XP_011523124.1:n.1336+25G>A
NM_000250.2:c.1621+25G>A MANE Select	NP_000241.1:n.1621+25G>A