Canonical Allele Identifier: CA2622386682

Gene: CENPJ RNF17

Linked Data

• gnomAD v4: 13-24883174-T-G

Genomic Alleles

HGVS	Genome Assembly
NC_000013.11:g.24883174T>G , CM000675.2:g.24883174T>G	GRCh38
NC_000013.10:g.25457312T>G , CM000675.1:g.25457312T>G	GRCh37
NC_000013.9:g.24355312T>G	NCBI36
NG_009165.2:g.44774A>C

Transcript Alleles

HGVS	Amino-acid change
ENST00000381884.9:c.*3A>C (CENPJ) MANE Select	ENSP00000371308.4:n.*3A>C
ENST00000545981.6:c.*760A>C (CENPJ)	ENSP00000441090.2:n.*760A>C
ENST00000381884.8:c.*3A>C (CENPJ)	ENSP00000371308.4:n.*3A>C
ENST00000545981.5:c.*761A>C (CENPJ)	ENSP00000441090.2:n.*761A>C
ENST00000616936.4:c.*674A>C (CENPJ)	ENSP00000477511.1:n.*674A>C
NM_018451.4:c.*3A>C (CENPJ)	NP_060921.3:n.*3A>C
NR_047594.1:n.4332A>C (CENPJ)
NR_047595.1:n.4130A>C (CENPJ)
XM_011535156.1:c.*10+3879T>G (RNF17)	XP_011533458.1:n.*10+3879T>G
XM_011535156.2:c.*10+3879T>G (RNF17)	XP_011533458.1:n.*10+3879T>G
NM_018451.5:c.*3A>C (CENPJ) MANE Select	NP_060921.3:n.*3A>C
NR_047594.2:n.4304A>C (CENPJ)
NR_047595.2:n.4102A>C (CENPJ)