Canonical Allele Identifier: CA2590256052

Gene: CENPJ RNF17

Linked Data

• gnomAD v3: 13-24882979-C-CAGGGTAGTGAATTATAAATG
• gnomAD v4: 13-24882979-C-CAGGGTAGTGAATTATAAATG

Genomic Alleles

HGVS	Genome Assembly
NC_000013.11:g.24882982_24883001dup , CM000675.2:g.24882982_24883001dup	GRCh38
NC_000013.10:g.25457120_25457139dup , CM000675.1:g.25457120_25457139dup	GRCh37
NC_000013.9:g.24355120_24355139dup	NCBI36
NG_009165.2:g.44949_44968dup

Transcript Alleles

HGVS	Amino-acid Change
ENST00000381884.9:c.*178_*197dup (CENPJ) MANE Select	ENSP00000371308.4:n.*178_*197dup
ENST00000616936.4:c.*849_*868dup (CENPJ)	ENSP00000477511.1:n.*849_*868dup
NM_018451.4:c.*178_*197dup (CENPJ)	NP_060921.3:n.*178_*197dup
NR_047594.1:n.4507_4526dup (CENPJ)
NR_047595.1:n.4305_4324dup (CENPJ)
XM_011535156.1:c.*10+3687_*10+3706dup (RNF17)	XP_011533458.1:n.*10+3687_*10+3706dup
XM_011535156.2:c.*10+3687_*10+3706dup (RNF17)	XP_011533458.1:n.*10+3687_*10+3706dup
NM_018451.5:c.*178_*197dup (CENPJ) MANE Select	NP_060921.3:n.*178_*197dup
NR_047594.2:n.4479_4498dup (CENPJ)
NR_047595.2:n.4277_4296dup (CENPJ)