Canonical Allele Identifier: CA2622386636

Gene: CENPJ RNF17

Linked Data

• gnomAD v4: 13-24883091-CAATA-C

Genomic Alleles

HGVS	Genome Assembly
NC_000013.11:g.24883095_24883098del , CM000675.2:g.24883095_24883098del	GRCh38
NC_000013.10:g.25457233_25457236del , CM000675.1:g.25457233_25457236del	GRCh37
NC_000013.9:g.24355233_24355236del	NCBI36
NG_009165.2:g.44853_44856del

Transcript Alleles

HGVS	Amino-acid Change
ENST00000381884.9:c.*82_*85del (CENPJ) MANE Select	ENSP00000371308.4:n.*82_*85del
ENST00000381884.8:c.*82_*85del (CENPJ)	ENSP00000371308.4:n.*82_*85del
ENST00000616936.4:c.*753_*756del (CENPJ)	ENSP00000477511.1:n.*753_*756del
NM_018451.4:c.*82_*85del (CENPJ)	NP_060921.3:n.*82_*85del
NR_047594.1:n.4411_4414del (CENPJ)
NR_047595.1:n.4209_4212del (CENPJ)
XM_011535156.1:c.*10+3800_*10+3803del (RNF17)	XP_011533458.1:n.*10+3800_*10+3803del
XM_011535156.2:c.*10+3800_*10+3803del (RNF17)	XP_011533458.1:n.*10+3800_*10+3803del
NM_018451.5:c.*82_*85del (CENPJ) MANE Select	NP_060921.3:n.*82_*85del
NR_047594.2:n.4383_4386del (CENPJ)
NR_047595.2:n.4181_4184del (CENPJ)