Canonical Allele Identifier: CA696759620

Gene: CENPJ RNF17

Linked Data

• dbSNP Id: rs1453153590
• gnomAD v3: 13-24883119-TG-T
• gnomAD v4: 13-24883119-TG-T
• MyVariant Identifiers: chr13:g.25457258del (hg19) ; chr13:g.24883120del (hg38)

Genomic Alleles

HGVS	Genome Assembly
NC_000013.11:g.24883120del , CM000675.2:g.24883120del	GRCh38
NC_000013.10:g.25457258del , CM000675.1:g.25457258del	GRCh37
NC_000013.9:g.24355258del	NCBI36
NG_009165.2:g.44828del

Transcript Alleles

HGVS	Amino-acid Change
ENST00000381884.9:c.*57del (CENPJ) MANE Select	ENSP00000371308.4:n.*57del
ENST00000381884.8:c.*57del (CENPJ)	ENSP00000371308.4:n.*57del
ENST00000616936.4:c.*728del (CENPJ)	ENSP00000477511.1:n.*728del
NM_018451.4:c.*57del (CENPJ)	NP_060921.3:n.*57del
NR_047594.1:n.4386del (CENPJ)
NR_047595.1:n.4184del (CENPJ)
XM_011535156.1:c.*10+3825del (RNF17)	XP_011533458.1:n.*10+3825del
XM_011535156.2:c.*10+3825del (RNF17)	XP_011533458.1:n.*10+3825del
NM_018451.5:c.*57del (CENPJ) MANE Select	NP_060921.3:n.*57del
NR_047594.2:n.4358del (CENPJ)
NR_047595.2:n.4156del (CENPJ)