Canonical Allele Identifier: CA696759551

Gene: CENPJ RNF17

Linked Data

• dbSNP Id: rs1277834170
• MyVariant Identifiers: chr13:g.25457209_25457210insTCT (hg19) ; chr13:g.24883071_24883072insTCT (hg38)

Genomic Alleles

HGVS	Genome Assembly
NC_000013.11:g.24883073_24883075dup , CM000675.2:g.24883073_24883075dup	GRCh38
NC_000013.10:g.25457211_25457213dup , CM000675.1:g.25457211_25457213dup	GRCh37
NC_000013.9:g.24355211_24355213dup	NCBI36
NG_009165.2:g.44874_44876dup

Transcript Alleles

HGVS	Amino-acid Change
ENST00000381884.9:c.*103_*105dup (CENPJ) MANE Select	ENSP00000371308.4:n.*103_*105dup
ENST00000381884.8:c.*103_*105dup (CENPJ)	ENSP00000371308.4:n.*103_*105dup
ENST00000616936.4:c.*774_*776dup (CENPJ)	ENSP00000477511.1:n.*774_*776dup
NM_018451.4:c.*103_*105dup (CENPJ)	NP_060921.3:n.*103_*105dup
NR_047594.1:n.4432_4434dup (CENPJ)
NR_047595.1:n.4230_4232dup (CENPJ)
XM_011535156.1:c.*10+3778_*10+3780dup (RNF17)	XP_011533458.1:n.*10+3778_*10+3780dup
XM_011535156.2:c.*10+3778_*10+3780dup (RNF17)	XP_011533458.1:n.*10+3778_*10+3780dup
NM_018451.5:c.*103_*105dup (CENPJ) MANE Select	NP_060921.3:n.*103_*105dup
NR_047594.2:n.4404_4406dup (CENPJ)
NR_047595.2:n.4202_4204dup (CENPJ)