Canonical Allele Identifier: CA2622386611

Gene: CENPJ RNF17

Linked Data

• gnomAD v4: 13-24883070-AATCT-A

Genomic Alleles

HGVS	Genome Assembly
NC_000013.11:g.24883071_24883074del , CM000675.2:g.24883071_24883074del	GRCh38
NC_000013.10:g.25457209_25457212del , CM000675.1:g.25457209_25457212del	GRCh37
NC_000013.9:g.24355209_24355212del	NCBI36
NG_009165.2:g.44874_44877del

Transcript Alleles

HGVS	Amino-acid Change
ENST00000381884.9:c.*103_*106del (CENPJ) MANE Select	ENSP00000371308.4:n.*103_*106del
ENST00000381884.8:c.*103_*106del (CENPJ)	ENSP00000371308.4:n.*103_*106del
ENST00000616936.4:c.*774_*777del (CENPJ)	ENSP00000477511.1:n.*774_*777del
NM_018451.4:c.*103_*106del (CENPJ)	NP_060921.3:n.*103_*106del
NR_047594.1:n.4432_4435del (CENPJ)
NR_047595.1:n.4230_4233del (CENPJ)
XM_011535156.1:c.*10+3776_*10+3779del (RNF17)	XP_011533458.1:n.*10+3776_*10+3779del
XM_011535156.2:c.*10+3776_*10+3779del (RNF17)	XP_011533458.1:n.*10+3776_*10+3779del
NM_018451.5:c.*103_*106del (CENPJ) MANE Select	NP_060921.3:n.*103_*106del
NR_047594.2:n.4404_4407del (CENPJ)
NR_047595.2:n.4202_4205del (CENPJ)