Canonical Allele Identifier: CA387594619

Gene: CENPJ RNF17

Linked Data

• COSMIC: COSM1706564
• MyVariant Identifiers: chr13:g.25457403G>A (hg19) ; chr13:g.24883265G>A (hg38)

Genomic Alleles

HGVS	Genome Assembly
NC_000013.11:g.24883265G>A , CM000675.2:g.24883265G>A	GRCh38
NC_000013.10:g.25457403G>A , CM000675.1:g.25457403G>A	GRCh37
NC_000013.9:g.24355403G>A	NCBI36
NG_009165.2:g.44683C>T

Transcript Alleles

HGVS	Amino-acid change
ENST00000381884.9:c.3929C>T (CENPJ) MANE Select	ENSP00000371308.4:p.Ala1310Val
ENST00000545981.6:c.*669C>T (CENPJ)	ENSP00000441090.2:n.*669C>T
ENST00000381884.8:c.3929C>T (CENPJ)	ENSP00000371308.4:p.Ala1310Val
ENST00000545981.5:c.*670C>T (CENPJ)	ENSP00000441090.2:n.*670C>T
ENST00000616936.4:c.*583C>T (CENPJ)	ENSP00000477511.1:n.*583C>T
NM_018451.4:c.3929C>T (CENPJ)	NP_060921.3:p.Ala1310Val
NR_047594.1:n.4241C>T (CENPJ)
NR_047595.1:n.4039C>T (CENPJ)
XM_011535156.1:c.*10+3970G>A (RNF17)	XP_011533458.1:n.*10+3970G>A
XM_011535156.2:c.*10+3970G>A (RNF17)	XP_011533458.1:n.*10+3970G>A
NM_018451.5:c.3929C>T (CENPJ) MANE Select	NP_060921.3:p.Ala1310Val
NR_047594.2:n.4213C>T (CENPJ)
NR_047595.2:n.4011C>T (CENPJ)