Canonical Allele Identifier: CA2079393935

Gene: CENPJ RNF17

Linked Data

• dbSNP Id: rs1953900443

Genomic Alleles

HGVS	Genome Assembly
NC_000013.11:g.24882865_24882873del , CM000675.2:g.24882865_24882873del	GRCh38
NC_000013.10:g.25457003_25457011del , CM000675.1:g.25457003_25457011del	GRCh37
NC_000013.9:g.24355003_24355011del	NCBI36
NG_009165.2:g.45077_45085del

Transcript Alleles

HGVS	Amino-acid Change
ENST00000381884.9:c.*306_*314del (CENPJ) MANE Select	ENSP00000371308.4:n.*306_*314del
ENST00000616936.4:c.*977_*985del (CENPJ)	ENSP00000477511.1:n.*977_*985del
NM_018451.4:c.*306_*314del (CENPJ)	NP_060921.3:n.*306_*314del
NR_047594.1:n.4635_4643del (CENPJ)
NR_047595.1:n.4433_4441del (CENPJ)
XM_011535156.1:c.*10+3570_*10+3578del (RNF17)	XP_011533458.1:n.*10+3570_*10+3578del
XM_011535156.2:c.*10+3570_*10+3578del (RNF17)	XP_011533458.1:n.*10+3570_*10+3578del
NM_018451.5:c.*306_*314del (CENPJ) MANE Select	NP_060921.3:n.*306_*314del
NR_047594.2:n.4607_4615del (CENPJ)
NR_047595.2:n.4405_4413del (CENPJ)