Canonical Allele Identifier: CA2079393924

Gene: CENPJ RNF17

Linked Data

• dbSNP Id: rs1953899965

Genomic Alleles

HGVS	Genome Assembly
NC_000013.11:g.24882853_24882855dup , CM000675.2:g.24882853_24882855dup	GRCh38
NC_000013.10:g.25456991_25456993dup , CM000675.1:g.25456991_25456993dup	GRCh37
NC_000013.9:g.24354991_24354993dup	NCBI36
NG_009165.2:g.45095_45097dup

Transcript Alleles

HGVS	Amino-acid Change
ENST00000381884.9:c.*324_*326dup (CENPJ) MANE Select	ENSP00000371308.4:n.*324_*326dup
ENST00000616936.4:c.*995_*997dup (CENPJ)	ENSP00000477511.1:n.*995_*997dup
NM_018451.4:c.*324_*326dup (CENPJ)	NP_060921.3:n.*324_*326dup
NR_047594.1:n.4653_4655dup (CENPJ)
NR_047595.1:n.4451_4453dup (CENPJ)
XM_011535156.1:c.*10+3558_*10+3560dup (RNF17)	XP_011533458.1:n.*10+3558_*10+3560dup
XM_011535156.2:c.*10+3558_*10+3560dup (RNF17)	XP_011533458.1:n.*10+3558_*10+3560dup
NM_018451.5:c.*324_*326dup (CENPJ) MANE Select	NP_060921.3:n.*324_*326dup
NR_047594.2:n.4625_4627dup (CENPJ)
NR_047595.2:n.4423_4425dup (CENPJ)