Canonical Allele Identifier: CA2079393979

Gene: CENPJ RNF17

Genomic Alleles

HGVS	Genome Assembly
NC_000013.11:g.24882904_24882906delinsAAC , CM000675.2:g.24882904_24882906delinsAAC	GRCh38
NC_000013.10:g.25457042_25457044delinsAAC , CM000675.1:g.25457042_25457044delinsAAC	GRCh37
NC_000013.9:g.24355042_24355044delinsAAC	NCBI36
NG_009165.2:g.45042_45044delinsGTT

Transcript Alleles

HGVS	Amino-acid Change
ENST00000381884.9:c.*271_*273delinsGTT (CENPJ) MANE Select	ENSP00000371308.4:n.*271_*273delinsGTT
ENST00000616936.4:c.*942_*944delinsGTT (CENPJ)	ENSP00000477511.1:n.*942_*944delinsGTT
NM_018451.4:c.*271_*273delinsGTT (CENPJ)	NP_060921.3:n.*271_*273delinsGTT
NR_047594.1:n.4600_4602delinsGTT (CENPJ)
NR_047595.1:n.4398_4400delinsGTT (CENPJ)
XM_011535156.1:c.*10+3609_*10+3611delinsAAC (RNF17)	XP_011533458.1:n.*10+3609_*10+3611delinsAAC
XM_011535156.2:c.*10+3609_*10+3611delinsAAC (RNF17)	XP_011533458.1:n.*10+3609_*10+3611delinsAAC
NM_018451.5:c.*271_*273delinsGTT (CENPJ) MANE Select	NP_060921.3:n.*271_*273delinsGTT
NR_047594.2:n.4572_4574delinsGTT (CENPJ)
NR_047595.2:n.4370_4372delinsGTT (CENPJ)