Canonical Allele Identifier: CA2622386537

Gene: CENPJ RNF17

Linked Data

• gnomAD v4: 13-24882977-GAC-G

Genomic Alleles

HGVS	Genome Assembly
NC_000013.11:g.24882979_24882980del , CM000675.2:g.24882979_24882980del	GRCh38
NC_000013.10:g.25457117_25457118del , CM000675.1:g.25457117_25457118del	GRCh37
NC_000013.9:g.24355117_24355118del	NCBI36
NG_009165.2:g.44969_44970del

Transcript Alleles

HGVS	Amino-acid Change
ENST00000381884.9:c.*198_*199del (CENPJ) MANE Select	ENSP00000371308.4:n.*198_*199del
ENST00000616936.4:c.*869_*870del (CENPJ)	ENSP00000477511.1:n.*869_*870del
NM_018451.4:c.*198_*199del (CENPJ)	NP_060921.3:n.*198_*199del
NR_047594.1:n.4527_4528del (CENPJ)
NR_047595.1:n.4325_4326del (CENPJ)
XM_011535156.1:c.*10+3684_*10+3685del (RNF17)	XP_011533458.1:n.*10+3684_*10+3685del
XM_011535156.2:c.*10+3684_*10+3685del (RNF17)	XP_011533458.1:n.*10+3684_*10+3685del
NM_018451.5:c.*198_*199del (CENPJ) MANE Select	NP_060921.3:n.*198_*199del
NR_047594.2:n.4499_4500del (CENPJ)
NR_047595.2:n.4297_4298del (CENPJ)