Canonical Allele Identifier: CA2622386673

Gene: CENPJ RNF17

Linked Data

• gnomAD v4: 13-24883151-GT-G

Genomic Alleles

HGVS	Genome Assembly
NC_000013.11:g.24883153del , CM000675.2:g.24883153del	GRCh38
NC_000013.10:g.25457291del , CM000675.1:g.25457291del	GRCh37
NC_000013.9:g.24355291del	NCBI36
NG_009165.2:g.44796del

Transcript Alleles

HGVS	Amino-acid Change
ENST00000381884.9:c.*25del (CENPJ) MANE Select	ENSP00000371308.4:n.*25del
ENST00000381884.8:c.*25del (CENPJ)	ENSP00000371308.4:n.*25del
ENST00000616936.4:c.*696del (CENPJ)	ENSP00000477511.1:n.*696del
NM_018451.4:c.*25del (CENPJ)	NP_060921.3:n.*25del
NR_047594.1:n.4354del (CENPJ)
NR_047595.1:n.4152del (CENPJ)
XM_011535156.1:c.*10+3858del (RNF17)	XP_011533458.1:n.*10+3858del
XM_011535156.2:c.*10+3858del (RNF17)	XP_011533458.1:n.*10+3858del
NM_018451.5:c.*25del (CENPJ) MANE Select	NP_060921.3:n.*25del
NR_047594.2:n.4326del (CENPJ)
NR_047595.2:n.4124del (CENPJ)