Canonical Allele Identifier: CA696759436

Gene: CENPJ RNF17

Linked Data

• dbSNP Id: rs1400263919
• MyVariant Identifiers: chr13:g.25457019T>C (hg19) ; chr13:g.24882881T>C (hg38)

Genomic Alleles

HGVS	Genome Assembly
NC_000013.11:g.24882881T>C , CM000675.2:g.24882881T>C	GRCh38
NC_000013.10:g.25457019T>C , CM000675.1:g.25457019T>C	GRCh37
NC_000013.9:g.24355019T>C	NCBI36
NG_009165.2:g.45067A>G

Transcript Alleles

HGVS	Amino-acid Change
ENST00000381884.9:c.*296A>G (CENPJ) MANE Select	ENSP00000371308.4:n.*296A>G
ENST00000616936.4:c.*967A>G (CENPJ)	ENSP00000477511.1:n.*967A>G
NM_018451.4:c.*296A>G (CENPJ)	NP_060921.3:n.*296A>G
NR_047594.1:n.4625A>G (CENPJ)
NR_047595.1:n.4423A>G (CENPJ)
XM_011535156.1:c.*10+3586T>C (RNF17)	XP_011533458.1:n.*10+3586T>C
XM_011535156.2:c.*10+3586T>C (RNF17)	XP_011533458.1:n.*10+3586T>C
NM_018451.5:c.*296A>G (CENPJ) MANE Select	NP_060921.3:n.*296A>G
NR_047594.2:n.4597A>G (CENPJ)
NR_047595.2:n.4395A>G (CENPJ)