Canonical Allele Identifier: CA919229888

Gene: CENPJ RNF17

Linked Data

• dbSNP Id: rs1555294416
• gnomAD v4: 13-24882870-CT-C

Genomic Alleles

HGVS	Genome Assembly
NC_000013.11:g.24882872del , CM000675.2:g.24882872del	GRCh38
NC_000013.10:g.25457010del , CM000675.1:g.25457010del	GRCh37
NC_000013.9:g.24355010del	NCBI36
NG_009165.2:g.45077del

Transcript Alleles

HGVS	Amino-acid Change
ENST00000381884.9:c.*306del (CENPJ) MANE Select	ENSP00000371308.4:n.*306del
ENST00000616936.4:c.*977del (CENPJ)	ENSP00000477511.1:n.*977del
NM_018451.4:c.*306del (CENPJ)	NP_060921.3:n.*306del
NR_047594.1:n.4635del (CENPJ)
NR_047595.1:n.4433del (CENPJ)
XM_011535156.1:c.*10+3577del (RNF17)	XP_011533458.1:n.*10+3577del
XM_011535156.2:c.*10+3577del (RNF17)	XP_011533458.1:n.*10+3577del
NM_018451.5:c.*306del (CENPJ) MANE Select	NP_060921.3:n.*306del
NR_047594.2:n.4607del (CENPJ)
NR_047595.2:n.4405del (CENPJ)