Canonical Allele Identifier: CA2622386641

Gene: CENPJ RNF17

Linked Data

• gnomAD v4: 13-24883099-TAAAC-T

Genomic Alleles

HGVS	Genome Assembly
NC_000013.11:g.24883101_24883104del , CM000675.2:g.24883101_24883104del	GRCh38
NC_000013.10:g.25457239_25457242del , CM000675.1:g.25457239_25457242del	GRCh37
NC_000013.9:g.24355239_24355242del	NCBI36
NG_009165.2:g.44845_44848del

Transcript Alleles

HGVS	Amino-acid Change
ENST00000381884.9:c.*74_*77del (CENPJ) MANE Select	ENSP00000371308.4:n.*74_*77del
ENST00000381884.8:c.*74_*77del (CENPJ)	ENSP00000371308.4:n.*74_*77del
ENST00000616936.4:c.*745_*748del (CENPJ)	ENSP00000477511.1:n.*745_*748del
NM_018451.4:c.*74_*77del (CENPJ)	NP_060921.3:n.*74_*77del
NR_047594.1:n.4403_4406del (CENPJ)
NR_047595.1:n.4201_4204del (CENPJ)
XM_011535156.1:c.*10+3806_*10+3809del (RNF17)	XP_011533458.1:n.*10+3806_*10+3809del
XM_011535156.2:c.*10+3806_*10+3809del (RNF17)	XP_011533458.1:n.*10+3806_*10+3809del
NM_018451.5:c.*74_*77del (CENPJ) MANE Select	NP_060921.3:n.*74_*77del
NR_047594.2:n.4375_4378del (CENPJ)
NR_047595.2:n.4173_4176del (CENPJ)