Canonical Allele Identifier: CA2079394048

Gene: CENPJ RNF17

Genomic Alleles

HGVS	Genome Assembly
NC_000013.11:g.24883069T= , CM000675.2:g.24883069T=	GRCh38
NC_000013.10:g.25457207T= , CM000675.1:g.25457207T=	GRCh37
NC_000013.9:g.24355207T=	NCBI36

Transcript Alleles

HGVS	Amino-acid Change
ENST00000381884.9:c.*108A= (CENPJ) MANE Select	ENSP00000371308.4:n.*108A=
ENST00000381884.8:c.*108A= (CENPJ)	ENSP00000371308.4:n.*108A=
ENST00000616936.4:c.*779A= (CENPJ)	ENSP00000477511.1:n.*779A=
XM_011535156.1:c.*10+3774T= (RNF17)	XP_011533458.1:n.*10+3774T=
XM_011535156.2:c.*10+3774T= (RNF17)	XP_011533458.1:n.*10+3774T=
NM_018451.5:c.*108A= (CENPJ) MANE Select	NP_060921.3:n.*108A=
NR_047594.2:n.4409A= (CENPJ)
NR_047595.2:n.4207A= (CENPJ)