Canonical Allele Identifier: CA2079393932

Gene: CENPJ RNF17

Linked Data

• dbSNP Id: rs1953900314

Genomic Alleles

HGVS	Genome Assembly
NC_000013.11:g.24882862del , CM000675.2:g.24882862del	GRCh38
NC_000013.10:g.25457000del , CM000675.1:g.25457000del	GRCh37
NC_000013.9:g.24355000del	NCBI36
NG_009165.2:g.45087del

Transcript Alleles

HGVS	Amino-acid Change
ENST00000381884.9:c.*316del (CENPJ) MANE Select	ENSP00000371308.4:n.*316del
ENST00000616936.4:c.*987del (CENPJ)	ENSP00000477511.1:n.*987del
NM_018451.4:c.*316del (CENPJ)	NP_060921.3:n.*316del
NR_047594.1:n.4645del (CENPJ)
NR_047595.1:n.4443del (CENPJ)
XM_011535156.1:c.*10+3567del (RNF17)	XP_011533458.1:n.*10+3567del
XM_011535156.2:c.*10+3567del (RNF17)	XP_011533458.1:n.*10+3567del
NM_018451.5:c.*316del (CENPJ) MANE Select	NP_060921.3:n.*316del
NR_047594.2:n.4617del (CENPJ)
NR_047595.2:n.4415del (CENPJ)