Canonical Allele Identifier: CA2079393926

Gene: CENPJ RNF17

Linked Data

• dbSNP Id: rs1410826367
• gnomAD v4: 13-24882851-T-G

Genomic Alleles

HGVS	Genome Assembly
NC_000013.11:g.24882851T>G , CM000675.2:g.24882851T>G	GRCh38
NC_000013.10:g.25456989T>G , CM000675.1:g.25456989T>G	GRCh37
NC_000013.9:g.24354989T>G	NCBI36
NG_009165.2:g.45097A>C

Transcript Alleles

HGVS	Amino-acid Change
ENST00000381884.9:c.*326A>C (CENPJ) MANE Select	ENSP00000371308.4:n.*326A>C
ENST00000616936.4:c.*997A>C (CENPJ)	ENSP00000477511.1:n.*997A>C
NM_018451.4:c.*326A>C (CENPJ)	NP_060921.3:n.*326A>C
NR_047594.1:n.4655A>C (CENPJ)
NR_047595.1:n.4453A>C (CENPJ)
XM_011535156.1:c.*10+3556T>G (RNF17)	XP_011533458.1:n.*10+3556T>G
XM_011535156.2:c.*10+3556T>G (RNF17)	XP_011533458.1:n.*10+3556T>G
NM_018451.5:c.*326A>C (CENPJ) MANE Select	NP_060921.3:n.*326A>C
NR_047594.2:n.4627A>C (CENPJ)
NR_047595.2:n.4425A>C (CENPJ)