Canonical Allele Identifier: CA2079393931

Gene: CENPJ RNF17

Genomic Alleles

HGVS	Genome Assembly
NC_000013.11:g.24882860_24882861delinsTC , CM000675.2:g.24882860_24882861delinsTC	GRCh38
NC_000013.10:g.25456998_25456999delinsTC , CM000675.1:g.25456998_25456999delinsTC	GRCh37
NC_000013.9:g.24354998_24354999delinsTC	NCBI36
NG_009165.2:g.45087_45088delinsGA

Transcript Alleles

HGVS	Amino-acid Change
ENST00000381884.9:c.*316_*317delinsGA (CENPJ) MANE Select	ENSP00000371308.4:n.*316_*317delinsGA
ENST00000616936.4:c.*987_*988delinsGA (CENPJ)	ENSP00000477511.1:n.*987_*988delinsGA
NM_018451.4:c.*316_*317delinsGA (CENPJ)	NP_060921.3:n.*316_*317delinsGA
NR_047594.1:n.4645_4646delinsGA (CENPJ)
NR_047595.1:n.4443_4444delinsGA (CENPJ)
XM_011535156.1:c.*10+3565_*10+3566delinsTC (RNF17)	XP_011533458.1:n.*10+3565_*10+3566delinsTC
XM_011535156.2:c.*10+3565_*10+3566delinsTC (RNF17)	XP_011533458.1:n.*10+3565_*10+3566delinsTC
NM_018451.5:c.*316_*317delinsGA (CENPJ) MANE Select	NP_060921.3:n.*316_*317delinsGA
NR_047594.2:n.4617_4618delinsGA (CENPJ)
NR_047595.2:n.4415_4416delinsGA (CENPJ)