Canonical Allele Identifier: CA696759602

Gene: CENPJ RNF17

Linked Data

• dbSNP Id: rs1170243276
• MyVariant Identifiers: chr13:g.25457247del (hg19) ; chr13:g.24883109del (hg38)

Genomic Alleles

HGVS	Genome Assembly
NC_000013.11:g.24883110del , CM000675.2:g.24883110del	GRCh38
NC_000013.10:g.25457248del , CM000675.1:g.25457248del	GRCh37
NC_000013.9:g.24355248del	NCBI36
NG_009165.2:g.44839del

Transcript Alleles

HGVS	Amino-acid Change
ENST00000381884.9:c.*68del (CENPJ) MANE Select	ENSP00000371308.4:n.*68del
ENST00000381884.8:c.*68del (CENPJ)	ENSP00000371308.4:n.*68del
ENST00000616936.4:c.*739del (CENPJ)	ENSP00000477511.1:n.*739del
NM_018451.4:c.*68del (CENPJ)	NP_060921.3:n.*68del
NR_047594.1:n.4397del (CENPJ)
NR_047595.1:n.4195del (CENPJ)
XM_011535156.1:c.*10+3815del (RNF17)	XP_011533458.1:n.*10+3815del
XM_011535156.2:c.*10+3815del (RNF17)	XP_011533458.1:n.*10+3815del
NM_018451.5:c.*68del (CENPJ) MANE Select	NP_060921.3:n.*68del
NR_047594.2:n.4369del (CENPJ)
NR_047595.2:n.4167del (CENPJ)