Canonical Allele Identifier: CA2798539591

Gene: CENPJ RNF17

Genomic Alleles

HGVS	Genome Assembly
NC_000013.11:g.24882887_24882890del , CM000675.2:g.24882887_24882890del	GRCh38
NC_000013.10:g.25457025_25457028del , CM000675.1:g.25457025_25457028del	GRCh37
NC_000013.9:g.24355025_24355028del	NCBI36
NG_009165.2:g.45059_45062del

Transcript Alleles

HGVS	Amino-acid Change
ENST00000381884.9:c.*288_*291del (CENPJ) MANE Select	ENSP00000371308.4:n.*288_*291del
ENST00000616936.4:c.*959_*962del (CENPJ)	ENSP00000477511.1:n.*959_*962del
NM_018451.4:c.*288_*291del (CENPJ)	NP_060921.3:n.*288_*291del
NR_047594.1:n.4617_4620del (CENPJ)
NR_047595.1:n.4415_4418del (CENPJ)
XM_011535156.1:c.*10+3592_*10+3595del (RNF17)	XP_011533458.1:n.*10+3592_*10+3595del
XM_011535156.2:c.*10+3592_*10+3595del (RNF17)	XP_011533458.1:n.*10+3592_*10+3595del
NM_018451.5:c.*288_*291del (CENPJ) MANE Select	NP_060921.3:n.*288_*291del
NR_047594.2:n.4589_4592del (CENPJ)
NR_047595.2:n.4387_4390del (CENPJ)