Canonical Allele Identifier: CA2622386612

Gene: CENPJ RNF17

Linked Data

• gnomAD v4: 13-24883071-A-ATCTT

Genomic Alleles

HGVS	Genome Assembly
NC_000013.11:g.24883073_24883076dup , CM000675.2:g.24883073_24883076dup	GRCh38
NC_000013.10:g.25457211_25457214dup , CM000675.1:g.25457211_25457214dup	GRCh37
NC_000013.9:g.24355211_24355214dup	NCBI36
NG_009165.2:g.44873_44876dup

Transcript Alleles

HGVS	Amino-acid Change
ENST00000381884.9:c.*102_*105dup (CENPJ) MANE Select	ENSP00000371308.4:n.*102_*105dup
ENST00000381884.8:c.*102_*105dup (CENPJ)	ENSP00000371308.4:n.*102_*105dup
ENST00000616936.4:c.*773_*776dup (CENPJ)	ENSP00000477511.1:n.*773_*776dup
NM_018451.4:c.*102_*105dup (CENPJ)	NP_060921.3:n.*102_*105dup
NR_047594.1:n.4431_4434dup (CENPJ)
NR_047595.1:n.4229_4232dup (CENPJ)
XM_011535156.1:c.*10+3778_*10+3781dup (RNF17)	XP_011533458.1:n.*10+3778_*10+3781dup
XM_011535156.2:c.*10+3778_*10+3781dup (RNF17)	XP_011533458.1:n.*10+3778_*10+3781dup
NM_018451.5:c.*102_*105dup (CENPJ) MANE Select	NP_060921.3:n.*102_*105dup
NR_047594.2:n.4403_4406dup (CENPJ)
NR_047595.2:n.4201_4204dup (CENPJ)