Canonical Allele Identifier: CA2622386663

Gene: CENPJ RNF17

Linked Data

• gnomAD v4: 13-24883135-TA-T

Genomic Alleles

HGVS	Genome Assembly
NC_000013.11:g.24883140del , CM000675.2:g.24883140del	GRCh38
NC_000013.10:g.25457278del , CM000675.1:g.25457278del	GRCh37
NC_000013.9:g.24355278del	NCBI36
NG_009165.2:g.44812del

Transcript Alleles

HGVS	Amino-acid Change
ENST00000381884.9:c.*41del (CENPJ) MANE Select	ENSP00000371308.4:n.*41del
ENST00000381884.8:c.*41del (CENPJ)	ENSP00000371308.4:n.*41del
ENST00000616936.4:c.*712del (CENPJ)	ENSP00000477511.1:n.*712del
NM_018451.4:c.*41del (CENPJ)	NP_060921.3:n.*41del
NR_047594.1:n.4370del (CENPJ)
NR_047595.1:n.4168del (CENPJ)
XM_011535156.1:c.*10+3845del (RNF17)	XP_011533458.1:n.*10+3845del
XM_011535156.2:c.*10+3845del (RNF17)	XP_011533458.1:n.*10+3845del
NM_018451.5:c.*41del (CENPJ) MANE Select	NP_060921.3:n.*41del
NR_047594.2:n.4342del (CENPJ)
NR_047595.2:n.4140del (CENPJ)