Canonical Allele Identifier: CA696759393

Gene: CENPJ RNF17

Linked Data

• dbSNP Id: rs796638364
• gnomAD v3: 13-24882866-A-ACTT
• gnomAD v4: 13-24882866-A-ACTT
• MyVariant Identifiers: chr13:g.25457004_25457005insCTT (hg19) ; chr13:g.24882866_24882867insCTT (hg38)

Genomic Alleles

HGVS	Genome Assembly
NC_000013.11:g.24882870_24882872dup , CM000675.2:g.24882870_24882872dup	GRCh38
NC_000013.10:g.25457008_25457010dup , CM000675.1:g.25457008_25457010dup	GRCh37
NC_000013.9:g.24355008_24355010dup	NCBI36
NG_009165.2:g.45079_45081dup

Transcript Alleles

HGVS	Amino-acid Change
ENST00000381884.9:c.*308_*310dup (CENPJ) MANE Select	ENSP00000371308.4:n.*308_*310dup
ENST00000616936.4:c.*979_*981dup (CENPJ)	ENSP00000477511.1:n.*979_*981dup
NM_018451.4:c.*308_*310dup (CENPJ)	NP_060921.3:n.*308_*310dup
NR_047594.1:n.4637_4639dup (CENPJ)
NR_047595.1:n.4435_4437dup (CENPJ)
XM_011535156.1:c.*10+3575_*10+3577dup (RNF17)	XP_011533458.1:n.*10+3575_*10+3577dup
XM_011535156.2:c.*10+3575_*10+3577dup (RNF17)	XP_011533458.1:n.*10+3575_*10+3577dup
NM_018451.5:c.*308_*310dup (CENPJ) MANE Select	NP_060921.3:n.*308_*310dup
NR_047594.2:n.4609_4611dup (CENPJ)
NR_047595.2:n.4407_4409dup (CENPJ)