Canonical Allele Identifier: CA608986608

Gene: CENPJ

Linked Data

• dbSNP Id: rs1064794036
• gnomAD v2: 13-25480007-CCTCT-C
• gnomAD v4: 13-24905869-CCTCT-C
• MyVariant Identifiers: chr13:g.25480008_25480011del (hg19) ; chr13:g.24905870_24905873del (hg38)

Genomic Alleles

HGVS	Genome Assembly
NC_000013.11:g.24905874_24905877del , CM000675.2:g.24905874_24905877del	GRCh38
NC_000013.10:g.25480012_25480015del , CM000675.1:g.25480012_25480015del	GRCh37
NC_000013.9:g.24378012_24378015del	NCBI36
NG_009165.2:g.22075_22078del

Transcript Alleles

HGVS	Amino-acid change
ENST00000381884.9:c.2165_2168del MANE Select	ENSP00000371308.4:p.Glu722GlyfsTer?
ENST00000545981.6:c.2165_2168del	ENSP00000441090.2:p.Glu722GlyfsTer?
ENST00000381884.8:c.2165_2168del	ENSP00000371308.4:p.Glu722GlyfsTer?
ENST00000545981.5:c.2165_2168del	ENSP00000441090.2:p.Glu722GlyfsTer?
ENST00000616936.4:c.2165_2168del	ENSP00000477511.1:p.Glu722GlyfsTer?
NM_018451.4:c.2165_2168del	NP_060921.3:p.Glu722GlyfsTer?
NR_047594.1:n.2360_2363del
NR_047595.1:n.2360_2363del
XM_011535149.1:c.2165_2168del	XP_011533451.1:p.Glu722GlyfsTer?
XM_011535150.1:c.2165_2168del	XP_011533452.1:p.Glu722GlyfsTer?
XM_011535151.1:c.2165_2168del	XP_011533453.1:p.Glu722GlyfsTer?
XR_941627.1:n.2360_2363del
XR_941628.1:n.2360_2363del
XM_011535149.2:c.2165_2168del	XP_011533451.1:p.Glu722GlyfsTer?
XM_011535150.2:c.2165_2168del	XP_011533452.1:p.Glu722GlyfsTer?
XM_017020673.1:c.2165_2168del	XP_016876162.1:p.Glu722GlyfsTer?
NM_018451.5:c.2165_2168del MANE Select	NP_060921.3:p.Glu722GlyfsTer?
NR_047594.2:n.2332_2335del
NR_047595.2:n.2332_2335del