Canonical Allele Identifier: CA2079393949

Gene: CENPJ RNF17

Genomic Alleles

HGVS	Genome Assembly
NC_000013.11:g.24882870_24882871delinsCT , CM000675.2:g.24882870_24882871delinsCT	GRCh38
NC_000013.10:g.25457008_25457009delinsCT , CM000675.1:g.25457008_25457009delinsCT	GRCh37
NC_000013.9:g.24355008_24355009delinsCT	NCBI36
NG_009165.2:g.45077_45078delinsAG

Transcript Alleles

HGVS	Amino-acid Change
ENST00000381884.9:c.*306_*307delinsAG (CENPJ) MANE Select	ENSP00000371308.4:n.*306_*307delinsAG
ENST00000616936.4:c.*977_*978delinsAG (CENPJ)	ENSP00000477511.1:n.*977_*978delinsAG
NM_018451.4:c.*306_*307delinsAG (CENPJ)	NP_060921.3:n.*306_*307delinsAG
NR_047594.1:n.4635_4636delinsAG (CENPJ)
NR_047595.1:n.4433_4434delinsAG (CENPJ)
XM_011535156.1:c.*10+3575_*10+3576delinsCT (RNF17)	XP_011533458.1:n.*10+3575_*10+3576delinsCT
XM_011535156.2:c.*10+3575_*10+3576delinsCT (RNF17)	XP_011533458.1:n.*10+3575_*10+3576delinsCT
NM_018451.5:c.*306_*307delinsAG (CENPJ) MANE Select	NP_060921.3:n.*306_*307delinsAG
NR_047594.2:n.4607_4608delinsAG (CENPJ)
NR_047595.2:n.4405_4406delinsAG (CENPJ)