Canonical Allele Identifier: CA2079394179

Gene: CENPJ RNF17

Genomic Alleles

HGVS	Genome Assembly
NC_000013.11:g.24883254_24883258delinsGATGA , CM000675.2:g.24883254_24883258delinsGATGA	GRCh38
NC_000013.10:g.25457392_25457396delinsGATGA , CM000675.1:g.25457392_25457396delinsGATGA	GRCh37
NC_000013.9:g.24355392_24355396delinsGATGA	NCBI36
NG_009165.2:g.44690_44694delinsTCATC

Transcript Alleles

HGVS	Amino-acid change
ENST00000381884.9:c.3936_3940delinsTCATC (CENPJ) MANE Select	ENSP00000371308.4:p.Gly1312=
ENST00000545981.6:c.*676_*680delinsTCATC (CENPJ)	ENSP00000441090.2:n.*676_*680delinsTCATC
ENST00000381884.8:c.3936_3940delinsTCATC (CENPJ)	ENSP00000371308.4:p.Gly1312=
ENST00000545981.5:c.*677_*681delinsTCATC (CENPJ)	ENSP00000441090.2:n.*677_*681delinsTCATC
ENST00000616936.4:c.*590_*594delinsTCATC (CENPJ)	ENSP00000477511.1:n.*590_*594delinsTCATC
NM_018451.4:c.3936_3940delinsTCATC (CENPJ)	NP_060921.3:p.Gly1312=
NR_047594.1:n.4248_4252delinsTCATC (CENPJ)
NR_047595.1:n.4046_4050delinsTCATC (CENPJ)
XM_011535156.1:c.*10+3959_*10+3963delinsGATGA (RNF17)	XP_011533458.1:n.*10+3959_*10+3963delinsG...
XM_011535156.2:c.*10+3959_*10+3963delinsGATGA (RNF17)	XP_011533458.1:n.*10+3959_*10+3963delinsG...
NM_018451.5:c.3936_3940delinsTCATC (CENPJ) MANE Select	NP_060921.3:p.Gly1312=
NR_047594.2:n.4220_4224delinsTCATC (CENPJ)
NR_047595.2:n.4018_4022delinsTCATC (CENPJ)