Canonical Allele Identifier: CA2079394216

Gene: CENPJ RNF17

Genomic Alleles

HGVS	Genome Assembly
NC_000013.11:g.24883338_24883341delinsCATT , CM000675.2:g.24883338_24883341delinsCATT	GRCh38
NC_000013.10:g.25457476_25457479delinsCATT , CM000675.1:g.25457476_25457479delinsCATT	GRCh37
NC_000013.9:g.24355476_24355479delinsCATT	NCBI36
NG_009165.2:g.44607_44610delinsAATG

Transcript Alleles

HGVS	Amino-acid Change
ENST00000381884.9:c.3853_3856delinsAATG (CENPJ) MANE Select	ENSP00000371308.4:p.Asn1285=
ENST00000545981.6:c.*593_*596delinsAATG (CENPJ)	ENSP00000441090.2:n.*593_*596delinsAATG
ENST00000381884.8:c.3853_3856delinsAATG (CENPJ)	ENSP00000371308.4:p.Asn1285=
ENST00000545981.5:c.*594_*597delinsAATG (CENPJ)	ENSP00000441090.2:n.*594_*597delinsAATG
ENST00000616936.4:c.*507_*510delinsAATG (CENPJ)	ENSP00000477511.1:n.*507_*510delinsAATG
NM_018451.4:c.3853_3856delinsAATG (CENPJ)	NP_060921.3:p.Asn1285=
NR_047594.1:n.4165_4168delinsAATG (CENPJ)
NR_047595.1:n.3963_3966delinsAATG (CENPJ)
XM_011535156.1:c.*10+4043_*10+4046delinsCATT (RNF17)	XP_011533458.1:n.*10+4043_*10+4046delinsCATT
XM_011535156.2:c.*10+4043_*10+4046delinsCATT (RNF17)	XP_011533458.1:n.*10+4043_*10+4046delinsCATT
NM_018451.5:c.3853_3856delinsAATG (CENPJ) MANE Select	NP_060921.3:p.Asn1285=
NR_047594.2:n.4137_4140delinsAATG (CENPJ)
NR_047595.2:n.3935_3938delinsAATG (CENPJ)