Canonical Allele Identifier: CA2079394125

Gene: CENPJ RNF17

Linked Data

• dbSNP Id: rs370679181
• gnomAD v4: 13-24883167-A-T

Genomic Alleles

HGVS	Genome Assembly
NC_000013.11:g.24883167A>T , CM000675.2:g.24883167A>T	GRCh38
NC_000013.10:g.25457305A>T , CM000675.1:g.25457305A>T	GRCh37
NC_000013.9:g.24355305A>T	NCBI36
NG_009165.2:g.44781T>A

Transcript Alleles

HGVS	Amino-acid change
ENST00000381884.9:c.*10T>A (CENPJ) MANE Select	ENSP00000371308.4:n.*10T>A
ENST00000545981.6:c.*767T>A (CENPJ)	ENSP00000441090.2:n.*767T>A
ENST00000381884.8:c.*10T>A (CENPJ)	ENSP00000371308.4:n.*10T>A
ENST00000545981.5:c.*768T>A (CENPJ)	ENSP00000441090.2:n.*768T>A
ENST00000616936.4:c.*681T>A (CENPJ)	ENSP00000477511.1:n.*681T>A
NM_018451.4:c.*10T>A (CENPJ)	NP_060921.3:n.*10T>A
NR_047594.1:n.4339T>A (CENPJ)
NR_047595.1:n.4137T>A (CENPJ)
XM_011535156.1:c.*10+3872A>T (RNF17)	XP_011533458.1:n.*10+3872A>T
XM_011535156.2:c.*10+3872A>T (RNF17)	XP_011533458.1:n.*10+3872A>T
NM_018451.5:c.*10T>A (CENPJ) MANE Select	NP_060921.3:n.*10T>A
NR_047594.2:n.4311T>A (CENPJ)
NR_047595.2:n.4109T>A (CENPJ)