Canonical Allele Identifier: CA2079393955

Gene: CENPJ RNF17

Linked Data

• dbSNP Id: rs138938177
• gnomAD v4: 13-24882874-GTT-G

Genomic Alleles

HGVS	Genome Assembly
NC_000013.11:g.24882882_24882883del , CM000675.2:g.24882882_24882883del	GRCh38
NC_000013.10:g.25457020_25457021del , CM000675.1:g.25457020_25457021del	GRCh37
NC_000013.9:g.24355020_24355021del	NCBI36
NG_009165.2:g.45072_45073del

Transcript Alleles

HGVS	Amino-acid Change
ENST00000381884.9:c.*301_*302del (CENPJ) MANE Select	ENSP00000371308.4:n.*301_*302del
ENST00000616936.4:c.*972_*973del (CENPJ)	ENSP00000477511.1:n.*972_*973del
NM_018451.4:c.*301_*302del (CENPJ)	NP_060921.3:n.*301_*302del
NR_047594.1:n.4630_4631del (CENPJ)
NR_047595.1:n.4428_4429del (CENPJ)
XM_011535156.1:c.*10+3587_*10+3588del (RNF17)	XP_011533458.1:n.*10+3587_*10+3588del
XM_011535156.2:c.*10+3587_*10+3588del (RNF17)	XP_011533458.1:n.*10+3587_*10+3588del
NM_018451.5:c.*301_*302del (CENPJ) MANE Select	NP_060921.3:n.*301_*302del
NR_047594.2:n.4602_4603del (CENPJ)
NR_047595.2:n.4400_4401del (CENPJ)