Canonical Allele Identifier: CA2079393975

Gene: CENPJ RNF17

Linked Data

• dbSNP Id: rs1953902517

Genomic Alleles

HGVS	Genome Assembly
NC_000013.11:g.24882902_24882905del , CM000675.2:g.24882902_24882905del	GRCh38
NC_000013.10:g.25457040_25457043del , CM000675.1:g.25457040_25457043del	GRCh37
NC_000013.9:g.24355040_24355043del	NCBI36
NG_009165.2:g.45045_45048del

Transcript Alleles

HGVS	Amino-acid Change
ENST00000381884.9:c.*274_*277del (CENPJ) MANE Select	ENSP00000371308.4:n.*274_*277del
ENST00000616936.4:c.*945_*948del (CENPJ)	ENSP00000477511.1:n.*945_*948del
NM_018451.4:c.*274_*277del (CENPJ)	NP_060921.3:n.*274_*277del
NR_047594.1:n.4603_4606del (CENPJ)
NR_047595.1:n.4401_4404del (CENPJ)
XM_011535156.1:c.*10+3607_*10+3610del (RNF17)	XP_011533458.1:n.*10+3607_*10+3610del
XM_011535156.2:c.*10+3607_*10+3610del (RNF17)	XP_011533458.1:n.*10+3607_*10+3610del
NM_018451.5:c.*274_*277del (CENPJ) MANE Select	NP_060921.3:n.*274_*277del
NR_047594.2:n.4575_4578del (CENPJ)
NR_047595.2:n.4373_4376del (CENPJ)