Canonical Allele Identifier: CA954159547

Gene: CENPJ RNF17

Linked Data

• dbSNP Id: rs1953901344
• gnomAD v3: 13-24882872-TG-T
• gnomAD v4: 13-24882872-TG-T

Genomic Alleles

HGVS	Genome Assembly
NC_000013.11:g.24882874del , CM000675.2:g.24882874del	GRCh38
NC_000013.10:g.25457012del , CM000675.1:g.25457012del	GRCh37
NC_000013.9:g.24355012del	NCBI36
NG_009165.2:g.45075del

Transcript Alleles

HGVS	Amino-acid Change
ENST00000381884.9:c.*304del (CENPJ) MANE Select	ENSP00000371308.4:n.*304del
ENST00000616936.4:c.*975del (CENPJ)	ENSP00000477511.1:n.*975del
NM_018451.4:c.*304del (CENPJ)	NP_060921.3:n.*304del
NR_047594.1:n.4633del (CENPJ)
NR_047595.1:n.4431del (CENPJ)
XM_011535156.1:c.*10+3579del (RNF17)	XP_011533458.1:n.*10+3579del
XM_011535156.2:c.*10+3579del (RNF17)	XP_011533458.1:n.*10+3579del
NM_018451.5:c.*304del (CENPJ) MANE Select	NP_060921.3:n.*304del
NR_047594.2:n.4605del (CENPJ)
NR_047595.2:n.4403del (CENPJ)