Canonical Allele Identifier: CA696759531

Gene: CENPJ RNF17

Linked Data

• dbSNP Id: rs1474732628
• gnomAD v3: 13-24883058-AT-A
• gnomAD v4: 13-24883058-AT-A
• MyVariant Identifiers: chr13:g.25457197del (hg19) ; chr13:g.24883059del (hg38)

Genomic Alleles

HGVS	Genome Assembly
NC_000013.11:g.24883062del , CM000675.2:g.24883062del	GRCh38
NC_000013.10:g.25457200del , CM000675.1:g.25457200del	GRCh37
NC_000013.9:g.24355200del	NCBI36
NG_009165.2:g.44889del

Transcript Alleles

HGVS	Amino-acid Change
ENST00000381884.9:c.*118del (CENPJ) MANE Select	ENSP00000371308.4:n.*118del
ENST00000381884.8:c.*118del (CENPJ)	ENSP00000371308.4:n.*118del
ENST00000616936.4:c.*789del (CENPJ)	ENSP00000477511.1:n.*789del
NM_018451.4:c.*118del (CENPJ)	NP_060921.3:n.*118del
NR_047594.1:n.4447del (CENPJ)
NR_047595.1:n.4245del (CENPJ)
XM_011535156.1:c.*10+3767del (RNF17)	XP_011533458.1:n.*10+3767del
XM_011535156.2:c.*10+3767del (RNF17)	XP_011533458.1:n.*10+3767del
NM_018451.5:c.*118del (CENPJ) MANE Select	NP_060921.3:n.*118del
NR_047594.2:n.4419del (CENPJ)
NR_047595.2:n.4217del (CENPJ)