Canonical Allele Identifier: CA954159614

Gene: CENPJ RNF17

Linked Data

• dbSNP Id: rs1953909055
• gnomAD v3: 13-24883124-A-AT
• gnomAD v4: 13-24883124-A-AT

Genomic Alleles

HGVS	Genome Assembly
NC_000013.11:g.24883130dup , CM000675.2:g.24883130dup	GRCh38
NC_000013.10:g.25457268dup , CM000675.1:g.25457268dup	GRCh37
NC_000013.9:g.24355268dup	NCBI36
NG_009165.2:g.44823dup

Transcript Alleles

HGVS	Amino-acid Change
ENST00000381884.9:c.*52dup (CENPJ) MANE Select	ENSP00000371308.4:n.*52dup
ENST00000381884.8:c.*52dup (CENPJ)	ENSP00000371308.4:n.*52dup
ENST00000616936.4:c.*723dup (CENPJ)	ENSP00000477511.1:n.*723dup
NM_018451.4:c.*52dup (CENPJ)	NP_060921.3:n.*52dup
NR_047594.1:n.4381dup (CENPJ)
NR_047595.1:n.4179dup (CENPJ)
XM_011535156.1:c.*10+3835dup (RNF17)	XP_011533458.1:n.*10+3835dup
XM_011535156.2:c.*10+3835dup (RNF17)	XP_011533458.1:n.*10+3835dup
NM_018451.5:c.*52dup (CENPJ) MANE Select	NP_060921.3:n.*52dup
NR_047594.2:n.4353dup (CENPJ)
NR_047595.2:n.4151dup (CENPJ)