Canonical Allele Identifier: CA2079393927

Gene: CENPJ RNF17

Linked Data

• dbSNP Id: rs1953900032

Genomic Alleles

HGVS	Genome Assembly
NC_000013.11:g.24882851_24882852insA , CM000675.2:g.24882851_24882852insA	GRCh38
NC_000013.10:g.25456989_25456990insA , CM000675.1:g.25456989_25456990insA	GRCh37
NC_000013.9:g.24354989_24354990insA	NCBI36
NG_009165.2:g.45096_45097insT

Transcript Alleles

HGVS	Amino-acid Change
ENST00000381884.9:c.*325_*326insT (CENPJ) MANE Select	ENSP00000371308.4:n.*325_*326insT
ENST00000616936.4:c.*996_*997insT (CENPJ)	ENSP00000477511.1:n.*996_*997insT
NM_018451.4:c.*325_*326insT (CENPJ)	NP_060921.3:n.*325_*326insT
NR_047594.1:n.4654_4655insT (CENPJ)
NR_047595.1:n.4452_4453insT (CENPJ)
XM_011535156.1:c.*10+3556_*10+3557insA (RNF17)	XP_011533458.1:n.*10+3556_*10+3557insA
XM_011535156.2:c.*10+3556_*10+3557insA (RNF17)	XP_011533458.1:n.*10+3556_*10+3557insA
NM_018451.5:c.*325_*326insT (CENPJ) MANE Select	NP_060921.3:n.*325_*326insT
NR_047594.2:n.4626_4627insT (CENPJ)
NR_047595.2:n.4424_4425insT (CENPJ)