Canonical Allele Identifier: CA387594622

Gene: CENPJ RNF17

Linked Data

• MyVariant Identifiers: chr13:g.25457404C>T (hg19) ; chr13:g.24883266C>T (hg38)

Genomic Alleles

HGVS	Genome Assembly
NC_000013.11:g.24883266C>T , CM000675.2:g.24883266C>T	GRCh38
NC_000013.10:g.25457404C>T , CM000675.1:g.25457404C>T	GRCh37
NC_000013.9:g.24355404C>T	NCBI36
NG_009165.2:g.44682G>A

Transcript Alleles

HGVS	Amino-acid change
ENST00000381884.9:c.3928G>A (CENPJ) MANE Select	ENSP00000371308.4:p.Ala1310Thr
ENST00000545981.6:c.*668G>A (CENPJ)	ENSP00000441090.2:n.*668G>A
ENST00000381884.8:c.3928G>A (CENPJ)	ENSP00000371308.4:p.Ala1310Thr
ENST00000545981.5:c.*669G>A (CENPJ)	ENSP00000441090.2:n.*669G>A
ENST00000616936.4:c.*582G>A (CENPJ)	ENSP00000477511.1:n.*582G>A
NM_018451.4:c.3928G>A (CENPJ)	NP_060921.3:p.Ala1310Thr
NR_047594.1:n.4240G>A (CENPJ)
NR_047595.1:n.4038G>A (CENPJ)
XM_011535156.1:c.*10+3971C>T (RNF17)	XP_011533458.1:n.*10+3971C>T
XM_011535156.2:c.*10+3971C>T (RNF17)	XP_011533458.1:n.*10+3971C>T
NM_018451.5:c.3928G>A (CENPJ) MANE Select	NP_060921.3:p.Ala1310Thr
NR_047594.2:n.4212G>A (CENPJ)
NR_047595.2:n.4010G>A (CENPJ)