Canonical Allele Identifier: CA2079394018

Gene: CENPJ RNF17

Genomic Alleles

HGVS	Genome Assembly
NC_000013.11:g.24882992_24882996delinsTATAA , CM000675.2:g.24882992_24882996delinsTATAA	GRCh38
NC_000013.10:g.25457130_25457134delinsTATAA , CM000675.1:g.25457130_25457134delinsTATAA	GRCh37
NC_000013.9:g.24355130_24355134delinsTATAA	NCBI36
NG_009165.2:g.44952_44956delinsTTATA

Transcript Alleles

HGVS	Amino-acid Change
ENST00000381884.9:c.*181_*185delinsTTATA (CENPJ) MANE Select	ENSP00000371308.4:n.*181_*185delinsTTATA
ENST00000616936.4:c.*852_*856delinsTTATA (CENPJ)	ENSP00000477511.1:n.*852_*856delinsTTATA
NM_018451.4:c.*181_*185delinsTTATA (CENPJ)	NP_060921.3:n.*181_*185delinsTTATA
NR_047594.1:n.4510_4514delinsTTATA (CENPJ)
NR_047595.1:n.4308_4312delinsTTATA (CENPJ)
XM_011535156.1:c.*10+3697_*10+3701delinsTATAA (RNF17)	XP_011533458.1:n.*10+3697_*10+3701delinsTATAA
XM_011535156.2:c.*10+3697_*10+3701delinsTATAA (RNF17)	XP_011533458.1:n.*10+3697_*10+3701delinsTATAA
NM_018451.5:c.*181_*185delinsTTATA (CENPJ) MANE Select	NP_060921.3:n.*181_*185delinsTTATA
NR_047594.2:n.4482_4486delinsTTATA (CENPJ)
NR_047595.2:n.4280_4284delinsTTATA (CENPJ)