Canonical Allele Identifier: CA247124015

Gene: CENPJ RNF17

Linked Data

• dbSNP Id: rs771835172
• gnomAD v3: 13-24882888-C-G
• gnomAD v4: 13-24882888-C-G
• MyVariant Identifiers: chr13:g.25457026C>G (hg19) ; chr13:g.24882888C>G (hg38)

Genomic Alleles

HGVS	Genome Assembly
NC_000013.11:g.24882888C>G , CM000675.2:g.24882888C>G	GRCh38
NC_000013.10:g.25457026C>G , CM000675.1:g.25457026C>G	GRCh37
NC_000013.9:g.24355026C>G	NCBI36
NG_009165.2:g.45060G>C

Transcript Alleles

HGVS	Amino-acid Change
ENST00000381884.9:c.*289G>C (CENPJ) MANE Select	ENSP00000371308.4:n.*289G>C
ENST00000616936.4:c.*960G>C (CENPJ)	ENSP00000477511.1:n.*960G>C
NM_018451.4:c.*289G>C (CENPJ)	NP_060921.3:n.*289G>C
NR_047594.1:n.4618G>C (CENPJ)
NR_047595.1:n.4416G>C (CENPJ)
XM_011535156.1:c.*10+3593C>G (RNF17)	XP_011533458.1:n.*10+3593C>G
XM_011535156.2:c.*10+3593C>G (RNF17)	XP_011533458.1:n.*10+3593C>G
NM_018451.5:c.*289G>C (CENPJ) MANE Select	NP_060921.3:n.*289G>C
NR_047594.2:n.4590G>C (CENPJ)
NR_047595.2:n.4388G>C (CENPJ)