Canonical Allele Identifier: CA2079394862

Gene: CENPJ RNF17

Genomic Alleles

HGVS	Genome Assembly
NC_000013.11:g.24884541C= , CM000675.2:g.24884541C=	GRCh38
NC_000013.10:g.25458679C= , CM000675.1:g.25458679C=	GRCh37
NC_000013.9:g.24356679C=	NCBI36
NG_009165.2:g.43407G=

Transcript Alleles

HGVS	Amino-acid Change
NM_018451.5:c.3478-78G= (CENPJ) MANE Select	NP_060921.3:n.3478-78G=
ENST00000381884.9:c.3478-78G= (CENPJ) MANE Select	ENSP00000371308.4:n.3478-78G=
NM_018451.4:c.3478-78G= (CENPJ)	NP_060921.3:n.3478-78G=
NR_047594.1:n.3790-78G= (CENPJ)
NR_047594.2:n.3762-78G= (CENPJ)
NR_047595.1:n.3588-78G= (CENPJ)
NR_047595.2:n.3560-78G= (CENPJ)
ENST00000381884.8:c.3478-78G= (CENPJ)	ENSP00000371308.4:n.3478-78G=
ENST00000471870.1:n.368-78G= (CENPJ)
ENST00000545981.5:c.*219-78G= (CENPJ)	ENSP00000441090.2:n.*219-78G=
ENST00000545981.6:c.*218-78G= (CENPJ)	ENSP00000441090.2:n.*218-78G=
ENST00000616936.4:c.*132-78G= (CENPJ)	ENSP00000477511.1:n.*132-78G=
XM_011535156.1:c.*11-3573C= (RNF17)	XP_011533458.1:n.*11-3573C=
XM_011535156.2:c.*11-3573C= (RNF17)	XP_011533458.1:n.*11-3573C=
XR_941627.1:n.3764-78G= (CENPJ)