Canonical Allele Identifier: CA2079394132

Gene: CENPJ RNF17

Linked Data

• dbSNP Id: rs1953911430

Genomic Alleles

HGVS	Genome Assembly
NC_000013.11:g.24883180_24883181del , CM000675.2:g.24883180_24883181del	GRCh38
NC_000013.10:g.25457318_25457319del , CM000675.1:g.25457318_25457319del	GRCh37
NC_000013.9:g.24355318_24355319del	NCBI36
NG_009165.2:g.44769_44770del

Transcript Alleles

HGVS	Amino-acid change
ENST00000381884.9:c.4015_4016del (CENPJ) MANE Select	ENSP00000371308.4:p.Ter1339ThrextTer5
ENST00000545981.6:c.*755_*756del (CENPJ)	ENSP00000441090.2:n.*755_*756del
ENST00000381884.8:c.4015_4016del (CENPJ)	ENSP00000371308.4:p.Ter1339ThrextTer5
ENST00000545981.5:c.*756_*757del (CENPJ)	ENSP00000441090.2:n.*756_*757del
ENST00000616936.4:c.*669_*670del (CENPJ)	ENSP00000477511.1:n.*669_*670del
NM_018451.4:c.4015_4016del (CENPJ)	NP_060921.3:p.Ter1339ThrextTer5
NR_047594.1:n.4327_4328del (CENPJ)
NR_047595.1:n.4125_4126del (CENPJ)
XM_011535156.1:c.*10+3885_*10+3886del (RNF17)	XP_011533458.1:n.*10+3885_*10+3886del
XM_011535156.2:c.*10+3885_*10+3886del (RNF17)	XP_011533458.1:n.*10+3885_*10+3886del
NM_018451.5:c.4015_4016del (CENPJ) MANE Select	NP_060921.3:p.Ter1339ThrextTer5
NR_047594.2:n.4299_4300del (CENPJ)
NR_047595.2:n.4097_4098del (CENPJ)