Canonical Allele Identifier: CA387594597

Gene: CENPJ RNF17

Linked Data

• gnomAD v4: 13-24883255-A-T
• COSMIC: COSM4046692
• MyVariant Identifiers: chr13:g.25457393A>T (hg19) ; chr13:g.24883255A>T (hg38)

Genomic Alleles

HGVS	Genome Assembly
NC_000013.11:g.24883255A>T , CM000675.2:g.24883255A>T	GRCh38
NC_000013.10:g.25457393A>T , CM000675.1:g.25457393A>T	GRCh37
NC_000013.9:g.24355393A>T	NCBI36
NG_009165.2:g.44693T>A

Transcript Alleles

HGVS	Amino-acid change
ENST00000381884.9:c.3939T>A (CENPJ) MANE Select	ENSP00000371308.4:p.His1313Gln
ENST00000545981.6:c.*679T>A (CENPJ)	ENSP00000441090.2:n.*679T>A
ENST00000381884.8:c.3939T>A (CENPJ)	ENSP00000371308.4:p.His1313Gln
ENST00000545981.5:c.*680T>A (CENPJ)	ENSP00000441090.2:n.*680T>A
ENST00000616936.4:c.*593T>A (CENPJ)	ENSP00000477511.1:n.*593T>A
NM_018451.4:c.3939T>A (CENPJ)	NP_060921.3:p.His1313Gln
NR_047594.1:n.4251T>A (CENPJ)
NR_047595.1:n.4049T>A (CENPJ)
XM_011535156.1:c.*10+3960A>T (RNF17)	XP_011533458.1:n.*10+3960A>T
XM_011535156.2:c.*10+3960A>T (RNF17)	XP_011533458.1:n.*10+3960A>T
NM_018451.5:c.3939T>A (CENPJ) MANE Select	NP_060921.3:p.His1313Gln
NR_047594.2:n.4223T>A (CENPJ)
NR_047595.2:n.4021T>A (CENPJ)