Canonical Allele Identifier: CA2839039790

Gene: CENPJ RNF17

Genomic Alleles

HGVS	Genome Assembly
NC_000013.11:g.24883359_24883360insAATAATG , CM000675.2:g.24883359_24883360insAATAATG	GRCh38
NC_000013.10:g.25457497_25457498insAATAATG , CM000675.1:g.25457497_25457498insAATAATG	GRCh37
NC_000013.9:g.24355497_24355498insAATAATG	NCBI36
NG_009165.2:g.44588_44589insCATTATT

Transcript Alleles

HGVS	Amino-acid Change
ENST00000381884.9:c.3834_3835insCATTATT (CENPJ) MANE Select	ENSP00000371308.4:p.Lys1279HisfsTer3
ENST00000545981.6:c.*574_*575insCATTATT (CENPJ)	ENSP00000441090.2:n.*574_*575insCATTATT
ENST00000381884.8:c.3834_3835insCATTATT (CENPJ)	ENSP00000371308.4:p.Lys1279HisfsTer3
ENST00000545981.5:c.*575_*576insCATTATT (CENPJ)	ENSP00000441090.2:n.*575_*576insCATTATT
ENST00000616936.4:c.*488_*489insCATTATT (CENPJ)	ENSP00000477511.1:n.*488_*489insCATTATT
NM_018451.4:c.3834_3835insCATTATT (CENPJ)	NP_060921.3:p.Lys1279HisfsTer3
NR_047594.1:n.4146_4147insCATTATT (CENPJ)
NR_047595.1:n.3944_3945insCATTATT (CENPJ)
XM_011535156.1:c.*10+4064_*10+4065insAATAATG (RNF17)	XP_011533458.1:n.*10+4064_*10+4065insAATAATG
XM_011535156.2:c.*10+4064_*10+4065insAATAATG (RNF17)	XP_011533458.1:n.*10+4064_*10+4065insAATAATG
NM_018451.5:c.3834_3835insCATTATT (CENPJ) MANE Select	NP_060921.3:p.Lys1279HisfsTer3
NR_047594.2:n.4118_4119insCATTATT (CENPJ)
NR_047595.2:n.3916_3917insCATTATT (CENPJ)