Canonical Allele Identifier: CA2622386489

Gene: CENPJ RNF17

Linked Data

• gnomAD v4: 13-24882905-A-C

Genomic Alleles

HGVS	Genome Assembly
NC_000013.11:g.24882905A>C , CM000675.2:g.24882905A>C	GRCh38
NC_000013.10:g.25457043A>C , CM000675.1:g.25457043A>C	GRCh37
NC_000013.9:g.24355043A>C	NCBI36
NG_009165.2:g.45043T>G

Transcript Alleles

HGVS	Amino-acid Change
ENST00000381884.9:c.*272T>G (CENPJ) MANE Select	ENSP00000371308.4:n.*272T>G
ENST00000616936.4:c.*943T>G (CENPJ)	ENSP00000477511.1:n.*943T>G
NM_018451.4:c.*272T>G (CENPJ)	NP_060921.3:n.*272T>G
NR_047594.1:n.4601T>G (CENPJ)
NR_047595.1:n.4399T>G (CENPJ)
XM_011535156.1:c.*10+3610A>C (RNF17)	XP_011533458.1:n.*10+3610A>C
XM_011535156.2:c.*10+3610A>C (RNF17)	XP_011533458.1:n.*10+3610A>C
NM_018451.5:c.*272T>G (CENPJ) MANE Select	NP_060921.3:n.*272T>G
NR_047594.2:n.4573T>G (CENPJ)
NR_047595.2:n.4371T>G (CENPJ)