Canonical Allele Identifier: CA2798539594

Gene: CENPJ RNF17

Genomic Alleles

HGVS	Genome Assembly
NC_000013.11:g.24882948_24882950dup , CM000675.2:g.24882948_24882950dup	GRCh38
NC_000013.10:g.25457086_25457088dup , CM000675.1:g.25457086_25457088dup	GRCh37
NC_000013.9:g.24355086_24355088dup	NCBI36
NG_009165.2:g.44998_45000dup

Transcript Alleles

HGVS	Amino-acid Change
ENST00000381884.9:c.*227_*229dup (CENPJ) MANE Select	ENSP00000371308.4:n.*227_*229dup
ENST00000616936.4:c.*898_*900dup (CENPJ)	ENSP00000477511.1:n.*898_*900dup
NM_018451.4:c.*227_*229dup (CENPJ)	NP_060921.3:n.*227_*229dup
NR_047594.1:n.4556_4558dup (CENPJ)
NR_047595.1:n.4354_4356dup (CENPJ)
XM_011535156.1:c.*10+3653_*10+3655dup (RNF17)	XP_011533458.1:n.*10+3653_*10+3655dup
XM_011535156.2:c.*10+3653_*10+3655dup (RNF17)	XP_011533458.1:n.*10+3653_*10+3655dup
NM_018451.5:c.*227_*229dup (CENPJ) MANE Select	NP_060921.3:n.*227_*229dup
NR_047594.2:n.4528_4530dup (CENPJ)
NR_047595.2:n.4326_4328dup (CENPJ)