Canonical Allele Identifier: CA773481963

Gene: MPO

Linked Data

• dbSNP Id: rs1214158913
• MyVariant Identifiers: chr17:g.56351055C>T (hg19) ; chr17:g.58273694C>T (hg38)

Genomic Alleles

HGVS	Genome Assembly
NC_000017.11:g.58273694C>T , CM000679.2:g.58273694C>T	GRCh38
NC_000017.10:g.56351055C>T , CM000679.1:g.56351055C>T	GRCh37
NC_000017.9:g.53706054C>T	NCBI36
NG_009629.1:g.12242G>A , LRG_84:g.12242G>A

Transcript Alleles

HGVS	Amino-acid Change
ENST00000578493.2:n.699-25G>A
ENST00000699291.1:c.491-25G>A	ENSP00000514272.1:n.491-25G>A
ENST00000699292.1:n.381G>A
ENST00000225275.4:c.1366-25G>A MANE Select	ENSP00000225275.3:n.1366-25G>A
ENST00000225275.3:c.1366-25G>A	ENSP00000225275.3:n.1366-25G>A
NM_000250.1:c.1366-25G>A , LRG_84t1:c.1366-25G>A	NP_000241.1:n.1366-25G>A
XM_011524821.1:c.1552-25G>A	XP_011523123.1:n.1552-25G>A
XM_011524822.1:c.1081-25G>A	XP_011523124.1:n.1081-25G>A
XM_011524823.1:c.1391-25G>A	XP_011523125.1:n.1391-25G>A
NM_000250.2:c.1366-25G>A MANE Select	NP_000241.1:n.1366-25G>A