Canonical Allele Identifier: CA2079394075

Gene: CENPJ RNF17

Genomic Alleles

HGVS	Genome Assembly
NC_000013.11:g.24883103_24883105delinsCAG , CM000675.2:g.24883103_24883105delinsCAG	GRCh38
NC_000013.10:g.25457241_25457243delinsCAG , CM000675.1:g.25457241_25457243delinsCAG	GRCh37
NC_000013.9:g.24355241_24355243delinsCAG	NCBI36
NG_009165.2:g.44843_44845delinsCTG

Transcript Alleles

HGVS	Amino-acid Change
ENST00000381884.9:c.*72_*74delinsCTG (CENPJ) MANE Select	ENSP00000371308.4:n.*72_*74delinsCTG
ENST00000381884.8:c.*72_*74delinsCTG (CENPJ)	ENSP00000371308.4:n.*72_*74delinsCTG
ENST00000616936.4:c.*743_*745delinsCTG (CENPJ)	ENSP00000477511.1:n.*743_*745delinsCTG
NM_018451.4:c.*72_*74delinsCTG (CENPJ)	NP_060921.3:n.*72_*74delinsCTG
NR_047594.1:n.4401_4403delinsCTG (CENPJ)
NR_047595.1:n.4199_4201delinsCTG (CENPJ)
XM_011535156.1:c.*10+3808_*10+3810delinsCAG (RNF17)	XP_011533458.1:n.*10+3808_*10+3810delinsCAG
XM_011535156.2:c.*10+3808_*10+3810delinsCAG (RNF17)	XP_011533458.1:n.*10+3808_*10+3810delinsCAG
NM_018451.5:c.*72_*74delinsCTG (CENPJ) MANE Select	NP_060921.3:n.*72_*74delinsCTG
NR_047594.2:n.4373_4375delinsCTG (CENPJ)
NR_047595.2:n.4171_4173delinsCTG (CENPJ)