Canonical Allele Identifier: CA2079394009

Gene: CENPJ RNF17

Linked Data

• dbSNP Id: rs1336544825
• gnomAD v4: 13-24882975-AAGAC-A

Genomic Alleles

HGVS	Genome Assembly
NC_000013.11:g.24882978_24882981del , CM000675.2:g.24882978_24882981del	GRCh38
NC_000013.10:g.25457116_25457119del , CM000675.1:g.25457116_25457119del	GRCh37
NC_000013.9:g.24355116_24355119del	NCBI36
NG_009165.2:g.44969_44972del

Transcript Alleles

HGVS	Amino-acid Change
ENST00000381884.9:c.*198_*201del (CENPJ) MANE Select	ENSP00000371308.4:n.*198_*201del
ENST00000616936.4:c.*869_*872del (CENPJ)	ENSP00000477511.1:n.*869_*872del
NM_018451.4:c.*198_*201del (CENPJ)	NP_060921.3:n.*198_*201del
NR_047594.1:n.4527_4530del (CENPJ)
NR_047595.1:n.4325_4328del (CENPJ)
XM_011535156.1:c.*10+3683_*10+3686del (RNF17)	XP_011533458.1:n.*10+3683_*10+3686del
XM_011535156.2:c.*10+3683_*10+3686del (RNF17)	XP_011533458.1:n.*10+3683_*10+3686del
NM_018451.5:c.*198_*201del (CENPJ) MANE Select	NP_060921.3:n.*198_*201del
NR_047594.2:n.4499_4502del (CENPJ)
NR_047595.2:n.4297_4300del (CENPJ)