Canonical Allele Identifier: CA2622386446

Gene: CENPJ RNF17

Linked Data

• gnomAD v4: 13-24882865-T-G

Genomic Alleles

HGVS	Genome Assembly
NC_000013.11:g.24882865T>G , CM000675.2:g.24882865T>G	GRCh38
NC_000013.10:g.25457003T>G , CM000675.1:g.25457003T>G	GRCh37
NC_000013.9:g.24355003T>G	NCBI36
NG_009165.2:g.45083A>C

Transcript Alleles

HGVS	Amino-acid Change
ENST00000381884.9:c.*312A>C (CENPJ) MANE Select	ENSP00000371308.4:n.*312A>C
ENST00000616936.4:c.*983A>C (CENPJ)	ENSP00000477511.1:n.*983A>C
NM_018451.4:c.*312A>C (CENPJ)	NP_060921.3:n.*312A>C
NR_047594.1:n.4641A>C (CENPJ)
NR_047595.1:n.4439A>C (CENPJ)
XM_011535156.1:c.*10+3570T>G (RNF17)	XP_011533458.1:n.*10+3570T>G
XM_011535156.2:c.*10+3570T>G (RNF17)	XP_011533458.1:n.*10+3570T>G
NM_018451.5:c.*312A>C (CENPJ) MANE Select	NP_060921.3:n.*312A>C
NR_047594.2:n.4613A>C (CENPJ)
NR_047595.2:n.4411A>C (CENPJ)