Canonical Allele Identifier: CA2622386634

Gene: CENPJ RNF17

Linked Data

• gnomAD v4: 13-24883087-T-TAC

Genomic Alleles

HGVS	Genome Assembly
NC_000013.11:g.24883091_24883092dup , CM000675.2:g.24883091_24883092dup	GRCh38
NC_000013.10:g.25457229_25457230dup , CM000675.1:g.25457229_25457230dup	GRCh37
NC_000013.9:g.24355229_24355230dup	NCBI36
NG_009165.2:g.44859_44860dup

Transcript Alleles

HGVS	Amino-acid Change
ENST00000381884.9:c.*88_*89dup (CENPJ) MANE Select	ENSP00000371308.4:n.*88_*89dup
ENST00000381884.8:c.*88_*89dup (CENPJ)	ENSP00000371308.4:n.*88_*89dup
ENST00000616936.4:c.*759_*760dup (CENPJ)	ENSP00000477511.1:n.*759_*760dup
NM_018451.4:c.*88_*89dup (CENPJ)	NP_060921.3:n.*88_*89dup
NR_047594.1:n.4417_4418dup (CENPJ)
NR_047595.1:n.4215_4216dup (CENPJ)
XM_011535156.1:c.*10+3796_*10+3797dup (RNF17)	XP_011533458.1:n.*10+3796_*10+3797dup
XM_011535156.2:c.*10+3796_*10+3797dup (RNF17)	XP_011533458.1:n.*10+3796_*10+3797dup
NM_018451.5:c.*88_*89dup (CENPJ) MANE Select	NP_060921.3:n.*88_*89dup
NR_047594.2:n.4389_4390dup (CENPJ)
NR_047595.2:n.4187_4188dup (CENPJ)