Canonical Allele Identifier: CA2622386617

Gene: CENPJ RNF17

Linked Data

• gnomAD v4: 13-24883077-T-TC

Genomic Alleles

HGVS	Genome Assembly
NC_000013.11:g.24883081dup , CM000675.2:g.24883081dup	GRCh38
NC_000013.10:g.25457219dup , CM000675.1:g.25457219dup	GRCh37
NC_000013.9:g.24355219dup	NCBI36
NG_009165.2:g.44870dup

Transcript Alleles

HGVS	Amino-acid Change
ENST00000381884.9:c.*99dup (CENPJ) MANE Select	ENSP00000371308.4:n.*99dup
ENST00000381884.8:c.*99dup (CENPJ)	ENSP00000371308.4:n.*99dup
ENST00000616936.4:c.*770dup (CENPJ)	ENSP00000477511.1:n.*770dup
NM_018451.4:c.*99dup (CENPJ)	NP_060921.3:n.*99dup
NR_047594.1:n.4428dup (CENPJ)
NR_047595.1:n.4226dup (CENPJ)
XM_011535156.1:c.*10+3786dup (RNF17)	XP_011533458.1:n.*10+3786dup
XM_011535156.2:c.*10+3786dup (RNF17)	XP_011533458.1:n.*10+3786dup
NM_018451.5:c.*99dup (CENPJ) MANE Select	NP_060921.3:n.*99dup
NR_047594.2:n.4400dup (CENPJ)
NR_047595.2:n.4198dup (CENPJ)