Canonical Allele Identifier: CA954159567

Gene: CENPJ RNF17

Linked Data

• dbSNP Id: rs1953903078
• gnomAD v3: 13-24882912-C-CACTT
• gnomAD v4: 13-24882912-C-CACTT

Genomic Alleles

HGVS	Genome Assembly
NC_000013.11:g.24882916_24882919dup , CM000675.2:g.24882916_24882919dup	GRCh38
NC_000013.10:g.25457054_25457057dup , CM000675.1:g.25457054_25457057dup	GRCh37
NC_000013.9:g.24355054_24355057dup	NCBI36
NG_009165.2:g.45032_45035dup

Transcript Alleles

HGVS	Amino-acid Change
ENST00000381884.9:c.*261_*264dup (CENPJ) MANE Select	ENSP00000371308.4:n.*261_*264dup
ENST00000616936.4:c.*932_*935dup (CENPJ)	ENSP00000477511.1:n.*932_*935dup
NM_018451.4:c.*261_*264dup (CENPJ)	NP_060921.3:n.*261_*264dup
NR_047594.1:n.4590_4593dup (CENPJ)
NR_047595.1:n.4388_4391dup (CENPJ)
XM_011535156.1:c.*10+3621_*10+3624dup (RNF17)	XP_011533458.1:n.*10+3621_*10+3624dup
XM_011535156.2:c.*10+3621_*10+3624dup (RNF17)	XP_011533458.1:n.*10+3621_*10+3624dup
NM_018451.5:c.*261_*264dup (CENPJ) MANE Select	NP_060921.3:n.*261_*264dup
NR_047594.2:n.4562_4565dup (CENPJ)
NR_047595.2:n.4360_4363dup (CENPJ)