Canonical Allele Identifier: CA954159565

Gene: CENPJ RNF17

Linked Data

• dbSNP Id: rs1953902780
• gnomAD v3: 13-24882904-AAC-A
• gnomAD v4: 13-24882904-AAC-A

Genomic Alleles

HGVS	Genome Assembly
NC_000013.11:g.24882909_24882910del , CM000675.2:g.24882909_24882910del	GRCh38
NC_000013.10:g.25457047_25457048del , CM000675.1:g.25457047_25457048del	GRCh37
NC_000013.9:g.24355047_24355048del	NCBI36
NG_009165.2:g.45042_45043del

Transcript Alleles

HGVS	Amino-acid Change
ENST00000381884.9:c.*271_*272del (CENPJ) MANE Select	ENSP00000371308.4:n.*271_*272del
ENST00000616936.4:c.*942_*943del (CENPJ)	ENSP00000477511.1:n.*942_*943del
NM_018451.4:c.*271_*272del (CENPJ)	NP_060921.3:n.*271_*272del
NR_047594.1:n.4600_4601del (CENPJ)
NR_047595.1:n.4398_4399del (CENPJ)
XM_011535156.1:c.*10+3614_*10+3615del (RNF17)	XP_011533458.1:n.*10+3614_*10+3615del
XM_011535156.2:c.*10+3614_*10+3615del (RNF17)	XP_011533458.1:n.*10+3614_*10+3615del
NM_018451.5:c.*271_*272del (CENPJ) MANE Select	NP_060921.3:n.*271_*272del
NR_047594.2:n.4572_4573del (CENPJ)
NR_047595.2:n.4370_4371del (CENPJ)