Canonical Allele Identifier: CA2798539588

Gene: CENPJ RNF17

Genomic Alleles

HGVS	Genome Assembly
NC_000013.11:g.24882878_24882883dup , CM000675.2:g.24882878_24882883dup	GRCh38
NC_000013.10:g.25457016_25457021dup , CM000675.1:g.25457016_25457021dup	GRCh37
NC_000013.9:g.24355016_24355021dup	NCBI36
NG_009165.2:g.45068_45073dup

Transcript Alleles

HGVS	Amino-acid Change
ENST00000381884.9:c.*297_*302dup (CENPJ) MANE Select	ENSP00000371308.4:n.*297_*302dup
ENST00000616936.4:c.*968_*973dup (CENPJ)	ENSP00000477511.1:n.*968_*973dup
NM_018451.4:c.*297_*302dup (CENPJ)	NP_060921.3:n.*297_*302dup
NR_047594.1:n.4626_4631dup (CENPJ)
NR_047595.1:n.4424_4429dup (CENPJ)
XM_011535156.1:c.*10+3583_*10+3588dup (RNF17)	XP_011533458.1:n.*10+3583_*10+3588dup
XM_011535156.2:c.*10+3583_*10+3588dup (RNF17)	XP_011533458.1:n.*10+3583_*10+3588dup
NM_018451.5:c.*297_*302dup (CENPJ) MANE Select	NP_060921.3:n.*297_*302dup
NR_047594.2:n.4598_4603dup (CENPJ)
NR_047595.2:n.4396_4401dup (CENPJ)