Canonical Allele Identifier: CA482981204

Gene: CENPJ RNF17

Linked Data

• MyVariant Identifiers: chr13:g.25457318C>G (hg19)

Genomic Alleles

HGVS	Genome Assembly
NC_000013.11:g.24883180C>G , CM000675.2:g.24883180C>G	GRCh38
NC_000013.10:g.25457318C>G , CM000675.1:g.25457318C>G	GRCh37
NC_000013.9:g.24355318C>G	NCBI36
NG_009165.2:g.44768G>C

Transcript Alleles

HGVS	Amino-acid change
ENST00000381884.9:c.4014G>C (CENPJ) MANE Select	ENSP00000371308.4:p.Leu1338=
ENST00000545981.6:c.*754G>C (CENPJ)	ENSP00000441090.2:n.*754G>C
ENST00000381884.8:c.4014G>C (CENPJ)	ENSP00000371308.4:p.Leu1338=
ENST00000545981.5:c.*755G>C (CENPJ)	ENSP00000441090.2:n.*755G>C
ENST00000616936.4:c.*668G>C (CENPJ)	ENSP00000477511.1:n.*668G>C
NM_018451.4:c.4014G>C (CENPJ)	NP_060921.3:p.Leu1338=
NR_047594.1:n.4326G>C (CENPJ)
NR_047595.1:n.4124G>C (CENPJ)
XM_011535156.1:c.*10+3885C>G (RNF17)	XP_011533458.1:n.*10+3885C>G
XM_011535156.2:c.*10+3885C>G (RNF17)	XP_011533458.1:n.*10+3885C>G
NM_018451.5:c.4014G>C (CENPJ) MANE Select	NP_060921.3:p.Leu1338=
NR_047594.2:n.4298G>C (CENPJ)
NR_047595.2:n.4096G>C (CENPJ)