Canonical Allele Identifier: CA608685719
Gene: CENPJ HGNC NCBI
RNF17 HGNC NCBI

Linked Data

dbSNP Id: rs138938177
gnomAD v2: 13-25457012-G-GT
gnomAD v3: 13-24882874-G-GT
gnomAD v4: 13-24882874-G-GT
MyVariant Identifiers: chr13:g.25457013_25457014insT (hg19) chr13:g.25457012_25457013insT (hg19) chr13:g.24882875_24882876insT (hg38) chr13:g.24882874_24882875insT (hg38)
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Genomic Alleles

HGVS Genome Assembly
NC_000013.11:g.24882883dup , CM000675.2:g.24882883dup GRCh38
NC_000013.10:g.25457021dup , CM000675.1:g.25457021dup GRCh37
NC_000013.9:g.24355021dup NCBI36
NG_009165.2:g.45073dup

Transcript Alleles

HGVS Amino-acid Change
ENST00000381884.9:c.*302dup (CENPJ) MANE Select ENSP00000371308.4:n.*302dup
ENST00000616936.4:c.*973dup (CENPJ) ENSP00000477511.1:n.*973dup
NM_018451.4:c.*302dup (CENPJ) NP_060921.3:n.*302dup
NR_047594.1:n.4631dup (CENPJ)
NR_047595.1:n.4429dup (CENPJ)
XM_011535156.1:c.*10+3588dup (RNF17) XP_011533458.1:n.*10+3588dup
XM_011535156.2:c.*10+3588dup (RNF17) XP_011533458.1:n.*10+3588dup
NM_018451.5:c.*302dup (CENPJ) MANE Select NP_060921.3:n.*302dup
NR_047594.2:n.4603dup (CENPJ)
NR_047595.2:n.4401dup (CENPJ)
Search 100 bp 5'
Search 100 bp 3'