Canonical Allele Identifier: CA696759574

Gene: CENPJ RNF17

Linked Data

• dbSNP Id: rs1212546672
• gnomAD v3: 13-24883084-A-ACAT
• gnomAD v4: 13-24883084-A-ACAT
• MyVariant Identifiers: chr13:g.25457222_25457223insCAT (hg19) ; chr13:g.24883084_24883085insCAT (hg38)

Genomic Alleles

HGVS	Genome Assembly
NC_000013.11:g.24883085_24883087dup , CM000675.2:g.24883085_24883087dup	GRCh38
NC_000013.10:g.25457223_25457225dup , CM000675.1:g.25457223_25457225dup	GRCh37
NC_000013.9:g.24355223_24355225dup	NCBI36
NG_009165.2:g.44861_44863dup

Transcript Alleles

HGVS	Amino-acid Change
ENST00000381884.9:c.*90_*92dup (CENPJ) MANE Select	ENSP00000371308.4:n.*90_*92dup
ENST00000381884.8:c.*90_*92dup (CENPJ)	ENSP00000371308.4:n.*90_*92dup
ENST00000616936.4:c.*761_*763dup (CENPJ)	ENSP00000477511.1:n.*761_*763dup
NM_018451.4:c.*90_*92dup (CENPJ)	NP_060921.3:n.*90_*92dup
NR_047594.1:n.4419_4421dup (CENPJ)
NR_047595.1:n.4217_4219dup (CENPJ)
XM_011535156.1:c.*10+3790_*10+3792dup (RNF17)	XP_011533458.1:n.*10+3790_*10+3792dup
XM_011535156.2:c.*10+3790_*10+3792dup (RNF17)	XP_011533458.1:n.*10+3790_*10+3792dup
NM_018451.5:c.*90_*92dup (CENPJ) MANE Select	NP_060921.3:n.*90_*92dup
NR_047594.2:n.4391_4393dup (CENPJ)
NR_047595.2:n.4189_4191dup (CENPJ)