Canonical Allele Identifier: CA2267631374

Gene: MPO

Linked Data

• dbSNP Id: rs1970398523

Genomic Alleles

HGVS	Genome Assembly
NC_000017.11:g.58273675_58273676insTGG , CM000679.2:g.58273675_58273676insTGG	GRCh38
NC_000017.10:g.56351036_56351037insTGG , CM000679.1:g.56351036_56351037insTGG	GRCh37
NC_000017.9:g.53706035_53706036insTGG	NCBI36
NG_009629.1:g.12261_12262insCAC , LRG_84:g.12261_12262insCAC

Transcript Alleles

HGVS	Amino-acid Change
ENST00000578493.2:n.699-6_699-5insCAC
ENST00000699291.1:c.491-6_491-5insCAC	ENSP00000514272.1:n.491-6_491-5insCAC
ENST00000699292.1:n.400_401insCAC
ENST00000225275.4:c.1366-6_1366-5insCAC MANE Select	ENSP00000225275.3:n.1366-6_1366-5insCAC
ENST00000225275.3:c.1366-6_1366-5insCAC	ENSP00000225275.3:n.1366-6_1366-5insCAC
NM_000250.1:c.1366-6_1366-5insCAC , LRG_84t1:c.1366-6_1366-5insCAC	NP_000241.1:n.1366-6_1366-5insCAC
XM_011524821.1:c.1552-6_1552-5insCAC	XP_011523123.1:n.1552-6_1552-5insCAC
XM_011524822.1:c.1081-6_1081-5insCAC	XP_011523124.1:n.1081-6_1081-5insCAC
XM_011524823.1:c.1391-6_1391-5insCAC	XP_011523125.1:n.1391-6_1391-5insCAC
NM_000250.2:c.1366-6_1366-5insCAC MANE Select	NP_000241.1:n.1366-6_1366-5insCAC