Canonical Allele Identifier: CA2622386615

Gene: CENPJ RNF17

Linked Data

• gnomAD v4: 13-24883073-CT-C

Genomic Alleles

HGVS	Genome Assembly
NC_000013.11:g.24883077del , CM000675.2:g.24883077del	GRCh38
NC_000013.10:g.25457215del , CM000675.1:g.25457215del	GRCh37
NC_000013.9:g.24355215del	NCBI36
NG_009165.2:g.44874del

Transcript Alleles

HGVS	Amino-acid Change
ENST00000381884.9:c.*103del (CENPJ) MANE Select	ENSP00000371308.4:n.*103del
ENST00000381884.8:c.*103del (CENPJ)	ENSP00000371308.4:n.*103del
ENST00000616936.4:c.*774del (CENPJ)	ENSP00000477511.1:n.*774del
NM_018451.4:c.*103del (CENPJ)	NP_060921.3:n.*103del
NR_047594.1:n.4432del (CENPJ)
NR_047595.1:n.4230del (CENPJ)
XM_011535156.1:c.*10+3782del (RNF17)	XP_011533458.1:n.*10+3782del
XM_011535156.2:c.*10+3782del (RNF17)	XP_011533458.1:n.*10+3782del
NM_018451.5:c.*103del (CENPJ) MANE Select	NP_060921.3:n.*103del
NR_047594.2:n.4404del (CENPJ)
NR_047595.2:n.4202del (CENPJ)