Canonical Allele Identifier: CA387594606

Gene: CENPJ RNF17

Linked Data

• MyVariant Identifiers: chr13:g.25457397C>G (hg19) ; chr13:g.24883259C>G (hg38)

Genomic Alleles

HGVS	Genome Assembly
NC_000013.11:g.24883259C>G , CM000675.2:g.24883259C>G	GRCh38
NC_000013.10:g.25457397C>G , CM000675.1:g.25457397C>G	GRCh37
NC_000013.9:g.24355397C>G	NCBI36
NG_009165.2:g.44689G>C

Transcript Alleles

HGVS	Amino-acid change
ENST00000381884.9:c.3935G>C (CENPJ) MANE Select	ENSP00000371308.4:p.Gly1312Ala
ENST00000545981.6:c.*675G>C (CENPJ)	ENSP00000441090.2:n.*675G>C
ENST00000381884.8:c.3935G>C (CENPJ)	ENSP00000371308.4:p.Gly1312Ala
ENST00000545981.5:c.*676G>C (CENPJ)	ENSP00000441090.2:n.*676G>C
ENST00000616936.4:c.*589G>C (CENPJ)	ENSP00000477511.1:n.*589G>C
NM_018451.4:c.3935G>C (CENPJ)	NP_060921.3:p.Gly1312Ala
NR_047594.1:n.4247G>C (CENPJ)
NR_047595.1:n.4045G>C (CENPJ)
XM_011535156.1:c.*10+3964C>G (RNF17)	XP_011533458.1:n.*10+3964C>G
XM_011535156.2:c.*10+3964C>G (RNF17)	XP_011533458.1:n.*10+3964C>G
NM_018451.5:c.3935G>C (CENPJ) MANE Select	NP_060921.3:p.Gly1312Ala
NR_047594.2:n.4219G>C (CENPJ)
NR_047595.2:n.4017G>C (CENPJ)