Canonical Allele Identifier: CA954159552

Gene: CENPJ RNF17

Linked Data

• gnomAD v3: 13-24882874-G-GTTT
• gnomAD v4: 13-24882874-G-GTTT

Genomic Alleles

HGVS	Genome Assembly
NC_000013.11:g.24882881_24882883dup , CM000675.2:g.24882881_24882883dup	GRCh38
NC_000013.10:g.25457019_25457021dup , CM000675.1:g.25457019_25457021dup	GRCh37
NC_000013.9:g.24355019_24355021dup	NCBI36
NG_009165.2:g.45071_45073dup

Transcript Alleles

HGVS	Amino-acid Change
ENST00000381884.9:c.*300_*302dup (CENPJ) MANE Select	ENSP00000371308.4:n.*300_*302dup
ENST00000616936.4:c.*971_*973dup (CENPJ)	ENSP00000477511.1:n.*971_*973dup
NM_018451.4:c.*300_*302dup (CENPJ)	NP_060921.3:n.*300_*302dup
NR_047594.1:n.4629_4631dup (CENPJ)
NR_047595.1:n.4427_4429dup (CENPJ)
XM_011535156.1:c.*10+3586_*10+3588dup (RNF17)	XP_011533458.1:n.*10+3586_*10+3588dup
XM_011535156.2:c.*10+3586_*10+3588dup (RNF17)	XP_011533458.1:n.*10+3586_*10+3588dup
NM_018451.5:c.*300_*302dup (CENPJ) MANE Select	NP_060921.3:n.*300_*302dup
NR_047594.2:n.4601_4603dup (CENPJ)
NR_047595.2:n.4399_4401dup (CENPJ)