Canonical Allele Identifier: CA2079393941

Gene: CENPJ RNF17

Linked Data

• dbSNP Id: rs1953900563

Genomic Alleles

HGVS	Genome Assembly
NC_000013.11:g.24882866_24882868del , CM000675.2:g.24882866_24882868del	GRCh38
NC_000013.10:g.25457004_25457006del , CM000675.1:g.25457004_25457006del	GRCh37
NC_000013.9:g.24355004_24355006del	NCBI36
NG_009165.2:g.45081_45083del

Transcript Alleles

HGVS	Amino-acid Change
ENST00000381884.9:c.*310_*312del (CENPJ) MANE Select	ENSP00000371308.4:n.*310_*312del
ENST00000616936.4:c.*981_*983del (CENPJ)	ENSP00000477511.1:n.*981_*983del
NM_018451.4:c.*310_*312del (CENPJ)	NP_060921.3:n.*310_*312del
NR_047594.1:n.4639_4641del (CENPJ)
NR_047595.1:n.4437_4439del (CENPJ)
XM_011535156.1:c.*10+3571_*10+3573del (RNF17)	XP_011533458.1:n.*10+3571_*10+3573del
XM_011535156.2:c.*10+3571_*10+3573del (RNF17)	XP_011533458.1:n.*10+3571_*10+3573del
NM_018451.5:c.*310_*312del (CENPJ) MANE Select	NP_060921.3:n.*310_*312del
NR_047594.2:n.4611_4613del (CENPJ)
NR_047595.2:n.4409_4411del (CENPJ)