Canonical Allele Identifier: CA2622386675

Gene: CENPJ RNF17

Linked Data

• gnomAD v4: 13-24883161-G-T

Genomic Alleles

HGVS	Genome Assembly
NC_000013.11:g.24883161G>T , CM000675.2:g.24883161G>T	GRCh38
NC_000013.10:g.25457299G>T , CM000675.1:g.25457299G>T	GRCh37
NC_000013.9:g.24355299G>T	NCBI36
NG_009165.2:g.44787C>A

Transcript Alleles

HGVS	Amino-acid Change
ENST00000381884.9:c.*16C>A (CENPJ) MANE Select	ENSP00000371308.4:n.*16C>A
ENST00000381884.8:c.*16C>A (CENPJ)	ENSP00000371308.4:n.*16C>A
ENST00000616936.4:c.*687C>A (CENPJ)	ENSP00000477511.1:n.*687C>A
NM_018451.4:c.*16C>A (CENPJ)	NP_060921.3:n.*16C>A
NR_047594.1:n.4345C>A (CENPJ)
NR_047595.1:n.4143C>A (CENPJ)
XM_011535156.1:c.*10+3866G>T (RNF17)	XP_011533458.1:n.*10+3866G>T
XM_011535156.2:c.*10+3866G>T (RNF17)	XP_011533458.1:n.*10+3866G>T
NM_018451.5:c.*16C>A (CENPJ) MANE Select	NP_060921.3:n.*16C>A
NR_047594.2:n.4317C>A (CENPJ)
NR_047595.2:n.4115C>A (CENPJ)