Canonical Allele Identifier: CA2622386457

Gene: CENPJ RNF17

Linked Data

• gnomAD v4: 13-24882874-G-GTTTTTTTTTTTT

Genomic Alleles

HGVS	Genome Assembly
NC_000013.11:g.24882883_24882884insTTTTTTTTTTTT , CM000675.2:g.24882883_24882884insTTTTTTTTTTTT	GRCh38
NC_000013.10:g.25457021_25457022insTTTTTTTTTTTT , CM000675.1:g.25457021_25457022insTTTTTTTTTTTT	GRCh37
NC_000013.9:g.24355021_24355022insTTTTTTTTTTTT	NCBI36
NG_009165.2:g.45073_45074insAAAAAAAAAAAA

Transcript Alleles

HGVS	Amino-acid Change
ENST00000381884.9:c.*302_*303insAAAAAAAAAAAA (CENPJ) MANE Select	ENSP00000371308.4:n.*302_*303insAAAAAAAAAAAA
ENST00000616936.4:c.*973_*974insAAAAAAAAAAAA (CENPJ)	ENSP00000477511.1:n.*973_*974insAAAAAAAAAAAA
NM_018451.4:c.*302_*303insAAAAAAAAAAAA (CENPJ)	NP_060921.3:n.*302_*303insAAAAAAAAAAAA
NR_047594.1:n.4631_4632insAAAAAAAAAAAA (CENPJ)
NR_047595.1:n.4429_4430insAAAAAAAAAAAA (CENPJ)
XM_011535156.1:c.*10+3588_*10+3589insTTTTTTTTTTTT (RNF17)	XP_011533458.1:n.*10+3588_*10+3589insTTTTTTTTTTTT
XM_011535156.2:c.*10+3588_*10+3589insTTTTTTTTTTTT (RNF17)	XP_011533458.1:n.*10+3588_*10+3589insTTTTTTTTTTTT
NM_018451.5:c.*302_*303insAAAAAAAAAAAA (CENPJ) MANE Select	NP_060921.3:n.*302_*303insAAAAAAAAAAAA
NR_047594.2:n.4603_4604insAAAAAAAAAAAA (CENPJ)
NR_047595.2:n.4401_4402insAAAAAAAAAAAA (CENPJ)