Canonical Allele Identifier: CA2079393967

Gene: CENPJ RNF17

Linked Data

• dbSNP Id: rs1953902276
• gnomAD v4: 13-24882889-C-CA

Genomic Alleles

HGVS	Genome Assembly
NC_000013.11:g.24882890dup , CM000675.2:g.24882890dup	GRCh38
NC_000013.10:g.25457028dup , CM000675.1:g.25457028dup	GRCh37
NC_000013.9:g.24355028dup	NCBI36
NG_009165.2:g.45058dup

Transcript Alleles

HGVS	Amino-acid Change
ENST00000381884.9:c.*287dup (CENPJ) MANE Select	ENSP00000371308.4:n.*287dup
ENST00000616936.4:c.*958dup (CENPJ)	ENSP00000477511.1:n.*958dup
NM_018451.4:c.*287dup (CENPJ)	NP_060921.3:n.*287dup
NR_047594.1:n.4616dup (CENPJ)
NR_047595.1:n.4414dup (CENPJ)
XM_011535156.1:c.*10+3595dup (RNF17)	XP_011533458.1:n.*10+3595dup
XM_011535156.2:c.*10+3595dup (RNF17)	XP_011533458.1:n.*10+3595dup
NM_018451.5:c.*287dup (CENPJ) MANE Select	NP_060921.3:n.*287dup
NR_047594.2:n.4588dup (CENPJ)
NR_047595.2:n.4386dup (CENPJ)