Canonical Allele Identifier: CA2622386555

Gene: CENPJ RNF17

Linked Data

• gnomAD v4: 13-24883022-G-A

Genomic Alleles

HGVS	Genome Assembly
NC_000013.11:g.24883022G>A , CM000675.2:g.24883022G>A	GRCh38
NC_000013.10:g.25457160G>A , CM000675.1:g.25457160G>A	GRCh37
NC_000013.9:g.24355160G>A	NCBI36
NG_009165.2:g.44926C>T

Transcript Alleles

HGVS	Amino-acid Change
ENST00000381884.9:c.*155C>T (CENPJ) MANE Select	ENSP00000371308.4:n.*155C>T
ENST00000616936.4:c.*826C>T (CENPJ)	ENSP00000477511.1:n.*826C>T
NM_018451.4:c.*155C>T (CENPJ)	NP_060921.3:n.*155C>T
NR_047594.1:n.4484C>T (CENPJ)
NR_047595.1:n.4282C>T (CENPJ)
XM_011535156.1:c.*10+3727G>A (RNF17)	XP_011533458.1:n.*10+3727G>A
XM_011535156.2:c.*10+3727G>A (RNF17)	XP_011533458.1:n.*10+3727G>A
NM_018451.5:c.*155C>T (CENPJ) MANE Select	NP_060921.3:n.*155C>T
NR_047594.2:n.4456C>T (CENPJ)
NR_047595.2:n.4254C>T (CENPJ)