Canonical Allele Identifier: CA627143259

Gene: MPO

Linked Data

• dbSNP Id: rs1457359656
• gnomAD v2: 17-56357865-C-T
• gnomAD v4: 17-58280504-C-T
• MyVariant Identifiers: chr17:g.56357865C>T (hg19) ; chr17:g.58280504C>T (hg38)

Genomic Alleles

HGVS	Genome Assembly
NC_000017.11:g.58280504C>T , CM000679.2:g.58280504C>T	GRCh38
NC_000017.10:g.56357865C>T , CM000679.1:g.56357865C>T	GRCh37
NC_000017.9:g.53712864C>T	NCBI36
NG_009629.1:g.5432G>A , LRG_84:g.5432G>A

Transcript Alleles

HGVS	Amino-acid Change
ENST00000225275.4:c.155-45G>A MANE Select	ENSP00000225275.3:n.155-45G>A
ENST00000225275.3:c.155-45G>A	ENSP00000225275.3:n.155-45G>A
ENST00000580005.1:n.84-45G>A
NM_000250.1:c.155-45G>A , LRG_84t1:c.155-45G>A	NP_000241.1:n.155-45G>A
XM_011524821.1:c.341-45G>A	XP_011523123.1:n.341-45G>A
XM_011524822.1:c.-38+101G>A	XP_011523124.1:n.-38+101G>A
XM_011524823.1:c.341-45G>A	XP_011523125.1:n.341-45G>A
NM_000250.2:c.155-45G>A MANE Select	NP_000241.1:n.155-45G>A