Canonical Allele Identifier: CA919229886

Gene: CENPJ RNF17

Linked Data

• dbSNP Id: rs398056195

Genomic Alleles

HGVS	Genome Assembly
NC_000013.11:g.24882870_24882871dup , CM000675.2:g.24882870_24882871dup	GRCh38
NC_000013.10:g.25457008_25457009dup , CM000675.1:g.25457008_25457009dup	GRCh37
NC_000013.9:g.24355008_24355009dup	NCBI36
NG_009165.2:g.45078_45079dup

Transcript Alleles

HGVS	Amino-acid Change
ENST00000381884.9:c.*307_*308dup (CENPJ) MANE Select	ENSP00000371308.4:n.*307_*308dup
ENST00000616936.4:c.*978_*979dup (CENPJ)	ENSP00000477511.1:n.*978_*979dup
NM_018451.4:c.*307_*308dup (CENPJ)	NP_060921.3:n.*307_*308dup
NR_047594.1:n.4636_4637dup (CENPJ)
NR_047595.1:n.4434_4435dup (CENPJ)
XM_011535156.1:c.*10+3575_*10+3576dup (RNF17)	XP_011533458.1:n.*10+3575_*10+3576dup
XM_011535156.2:c.*10+3575_*10+3576dup (RNF17)	XP_011533458.1:n.*10+3575_*10+3576dup
NM_018451.5:c.*307_*308dup (CENPJ) MANE Select	NP_060921.3:n.*307_*308dup
NR_047594.2:n.4608_4609dup (CENPJ)
NR_047595.2:n.4406_4407dup (CENPJ)