Canonical Allele Identifier: CA2622386584

Gene: CENPJ RNF17

Linked Data

• gnomAD v4: 13-24883049-TA-T

Genomic Alleles

HGVS	Genome Assembly
NC_000013.11:g.24883052del , CM000675.2:g.24883052del	GRCh38
NC_000013.10:g.25457190del , CM000675.1:g.25457190del	GRCh37
NC_000013.9:g.24355190del	NCBI36
NG_009165.2:g.44898del

Transcript Alleles

HGVS	Amino-acid Change
ENST00000381884.9:c.*127del (CENPJ) MANE Select	ENSP00000371308.4:n.*127del
ENST00000381884.8:c.*127del (CENPJ)	ENSP00000371308.4:n.*127del
ENST00000616936.4:c.*798del (CENPJ)	ENSP00000477511.1:n.*798del
NM_018451.4:c.*127del (CENPJ)	NP_060921.3:n.*127del
NR_047594.1:n.4456del (CENPJ)
NR_047595.1:n.4254del (CENPJ)
XM_011535156.1:c.*10+3757del (RNF17)	XP_011533458.1:n.*10+3757del
XM_011535156.2:c.*10+3757del (RNF17)	XP_011533458.1:n.*10+3757del
NM_018451.5:c.*127del (CENPJ) MANE Select	NP_060921.3:n.*127del
NR_047594.2:n.4428del (CENPJ)
NR_047595.2:n.4226del (CENPJ)