Canonical Allele Identifier: CA954159569

Gene: CENPJ RNF17

Linked Data

• dbSNP Id: rs147198592
• gnomAD v3: 13-24882914-C-A
• gnomAD v4: 13-24882914-C-A

Genomic Alleles

HGVS	Genome Assembly
NC_000013.11:g.24882914C>A , CM000675.2:g.24882914C>A	GRCh38
NC_000013.10:g.25457052C>A , CM000675.1:g.25457052C>A	GRCh37
NC_000013.9:g.24355052C>A	NCBI36
NG_009165.2:g.45034G>T

Transcript Alleles

HGVS	Amino-acid Change
ENST00000381884.9:c.*263G>T (CENPJ) MANE Select	ENSP00000371308.4:n.*263G>T
ENST00000616936.4:c.*934G>T (CENPJ)	ENSP00000477511.1:n.*934G>T
NM_018451.4:c.*263G>T (CENPJ)	NP_060921.3:n.*263G>T
NR_047594.1:n.4592G>T (CENPJ)
NR_047595.1:n.4390G>T (CENPJ)
XM_011535156.1:c.*10+3619C>A (RNF17)	XP_011533458.1:n.*10+3619C>A
XM_011535156.2:c.*10+3619C>A (RNF17)	XP_011533458.1:n.*10+3619C>A
NM_018451.5:c.*263G>T (CENPJ) MANE Select	NP_060921.3:n.*263G>T
NR_047594.2:n.4564G>T (CENPJ)
NR_047595.2:n.4362G>T (CENPJ)