Canonical Allele Identifier: CA2622386454

Gene: CENPJ RNF17

Linked Data

• gnomAD v4: 13-24882872-TGG-T

Genomic Alleles

HGVS	Genome Assembly
NC_000013.11:g.24882873_24882874del , CM000675.2:g.24882873_24882874del	GRCh38
NC_000013.10:g.25457011_25457012del , CM000675.1:g.25457011_25457012del	GRCh37
NC_000013.9:g.24355011_24355012del	NCBI36
NG_009165.2:g.45074_45075del

Transcript Alleles

HGVS	Amino-acid Change
ENST00000381884.9:c.*303_*304del (CENPJ) MANE Select	ENSP00000371308.4:n.*303_*304del
ENST00000616936.4:c.*974_*975del (CENPJ)	ENSP00000477511.1:n.*974_*975del
NM_018451.4:c.*303_*304del (CENPJ)	NP_060921.3:n.*303_*304del
NR_047594.1:n.4632_4633del (CENPJ)
NR_047595.1:n.4430_4431del (CENPJ)
XM_011535156.1:c.*10+3578_*10+3579del (RNF17)	XP_011533458.1:n.*10+3578_*10+3579del
XM_011535156.2:c.*10+3578_*10+3579del (RNF17)	XP_011533458.1:n.*10+3578_*10+3579del
NM_018451.5:c.*303_*304del (CENPJ) MANE Select	NP_060921.3:n.*303_*304del
NR_047594.2:n.4604_4605del (CENPJ)
NR_047595.2:n.4402_4403del (CENPJ)