Canonical Allele Identifier: CA482982097

Gene: CENPJ RNF17

Linked Data

• MyVariant Identifiers: chr13:g.25457438C>A (hg19)

Genomic Alleles

HGVS	Genome Assembly
NC_000013.11:g.24883300C>A , CM000675.2:g.24883300C>A	GRCh38
NC_000013.10:g.25457438C>A , CM000675.1:g.25457438C>A	GRCh37
NC_000013.9:g.24355438C>A	NCBI36
NG_009165.2:g.44648G>T

Transcript Alleles

HGVS	Amino-acid Change
ENST00000381884.9:c.3894G>T (CENPJ) MANE Select	ENSP00000371308.4:p.Arg1298=
ENST00000545981.6:c.*634G>T (CENPJ)	ENSP00000441090.2:n.*634G>T
ENST00000381884.8:c.3894G>T (CENPJ)	ENSP00000371308.4:p.Arg1298=
ENST00000545981.5:c.*635G>T (CENPJ)	ENSP00000441090.2:n.*635G>T
ENST00000616936.4:c.*548G>T (CENPJ)	ENSP00000477511.1:n.*548G>T
NM_018451.4:c.3894G>T (CENPJ)	NP_060921.3:p.Arg1298=
NR_047594.1:n.4206G>T (CENPJ)
NR_047595.1:n.4004G>T (CENPJ)
XM_011535156.1:c.*10+4005C>A (RNF17)	XP_011533458.1:n.*10+4005C>A
XM_011535156.2:c.*10+4005C>A (RNF17)	XP_011533458.1:n.*10+4005C>A
NM_018451.5:c.3894G>T (CENPJ) MANE Select	NP_060921.3:p.Arg1298=
NR_047594.2:n.4178G>T (CENPJ)
NR_047595.2:n.3976G>T (CENPJ)