Canonical Allele Identifier: CA954159601

Gene: CENPJ RNF17

Linked Data

• dbSNP Id: rs1953907236
• gnomAD v3: 13-24883083-C-CACAT
• gnomAD v4: 13-24883083-C-CACAT

Genomic Alleles

HGVS	Genome Assembly
NC_000013.11:g.24883087_24883090dup , CM000675.2:g.24883087_24883090dup	GRCh38
NC_000013.10:g.25457225_25457228dup , CM000675.1:g.25457225_25457228dup	GRCh37
NC_000013.9:g.24355225_24355228dup	NCBI36
NG_009165.2:g.44861_44864dup

Transcript Alleles

HGVS	Amino-acid Change
ENST00000381884.9:c.*90_*93dup (CENPJ) MANE Select	ENSP00000371308.4:n.*90_*93dup
ENST00000381884.8:c.*90_*93dup (CENPJ)	ENSP00000371308.4:n.*90_*93dup
ENST00000616936.4:c.*761_*764dup (CENPJ)	ENSP00000477511.1:n.*761_*764dup
NM_018451.4:c.*90_*93dup (CENPJ)	NP_060921.3:n.*90_*93dup
NR_047594.1:n.4419_4422dup (CENPJ)
NR_047595.1:n.4217_4220dup (CENPJ)
XM_011535156.1:c.*10+3792_*10+3795dup (RNF17)	XP_011533458.1:n.*10+3792_*10+3795dup
XM_011535156.2:c.*10+3792_*10+3795dup (RNF17)	XP_011533458.1:n.*10+3792_*10+3795dup
NM_018451.5:c.*90_*93dup (CENPJ) MANE Select	NP_060921.3:n.*90_*93dup
NR_047594.2:n.4391_4394dup (CENPJ)
NR_047595.2:n.4189_4192dup (CENPJ)