Canonical Allele Identifier: CA6919064

Gene: CENPJ RNF17

Linked Data

• dbSNP Id: rs755289851
• ExAC: 13:25457296 C / T
• gnomAD v2: 13-25457296-C-T
• gnomAD v4: 13-24883158-C-T
• MyVariant Identifiers: chr13:g.25457296C>T (hg19) ; chr13:g.24883158C>T (hg38)

Genomic Alleles

HGVS	Genome Assembly
NC_000013.11:g.24883158C>T , CM000675.2:g.24883158C>T	GRCh38
NC_000013.10:g.25457296C>T , CM000675.1:g.25457296C>T	GRCh37
NC_000013.9:g.24355296C>T	NCBI36
NG_009165.2:g.44790G>A

Transcript Alleles

HGVS	Amino-acid change
ENST00000381884.9:c.*19G>A (CENPJ) MANE Select	ENSP00000371308.4:n.*19G>A
ENST00000381884.8:c.*19G>A (CENPJ)	ENSP00000371308.4:n.*19G>A
ENST00000616936.4:c.*690G>A (CENPJ)	ENSP00000477511.1:n.*690G>A
NM_018451.4:c.*19G>A (CENPJ)	NP_060921.3:n.*19G>A
NR_047594.1:n.4348G>A (CENPJ)
NR_047595.1:n.4146G>A (CENPJ)
XM_011535156.1:c.*10+3863C>T (RNF17)	XP_011533458.1:n.*10+3863C>T
XM_011535156.2:c.*10+3863C>T (RNF17)	XP_011533458.1:n.*10+3863C>T
NM_018451.5:c.*19G>A (CENPJ) MANE Select	NP_060921.3:n.*19G>A
NR_047594.2:n.4320G>A (CENPJ)
NR_047595.2:n.4118G>A (CENPJ)