Canonical Allele Identifier: CA482981553

Gene: CENPJ RNF17

Linked Data

• MyVariant Identifiers: chr13:g.25457396A>G (hg19)

Genomic Alleles

HGVS	Genome Assembly
NC_000013.11:g.24883258A>G , CM000675.2:g.24883258A>G	GRCh38
NC_000013.10:g.25457396A>G , CM000675.1:g.25457396A>G	GRCh37
NC_000013.9:g.24355396A>G	NCBI36
NG_009165.2:g.44690T>C

Transcript Alleles

HGVS	Amino-acid change
ENST00000381884.9:c.3936T>C (CENPJ) MANE Select	ENSP00000371308.4:p.Gly1312=
ENST00000545981.6:c.*676T>C (CENPJ)	ENSP00000441090.2:n.*676T>C
ENST00000381884.8:c.3936T>C (CENPJ)	ENSP00000371308.4:p.Gly1312=
ENST00000545981.5:c.*677T>C (CENPJ)	ENSP00000441090.2:n.*677T>C
ENST00000616936.4:c.*590T>C (CENPJ)	ENSP00000477511.1:n.*590T>C
NM_018451.4:c.3936T>C (CENPJ)	NP_060921.3:p.Gly1312=
NR_047594.1:n.4248T>C (CENPJ)
NR_047595.1:n.4046T>C (CENPJ)
XM_011535156.1:c.*10+3963A>G (RNF17)	XP_011533458.1:n.*10+3963A>G
XM_011535156.2:c.*10+3963A>G (RNF17)	XP_011533458.1:n.*10+3963A>G
NM_018451.5:c.3936T>C (CENPJ) MANE Select	NP_060921.3:p.Gly1312=
NR_047594.2:n.4220T>C (CENPJ)
NR_047595.2:n.4018T>C (CENPJ)