Canonical Allele Identifier: CA2079393944

Gene: CENPJ RNF17

Genomic Alleles

HGVS	Genome Assembly
NC_000013.11:g.24882866_24882869delinsACTT , CM000675.2:g.24882866_24882869delinsACTT	GRCh38
NC_000013.10:g.25457004_25457007delinsACTT , CM000675.1:g.25457004_25457007delinsACTT	GRCh37
NC_000013.9:g.24355004_24355007delinsACTT	NCBI36
NG_009165.2:g.45079_45082delinsAAGT

Transcript Alleles

HGVS	Amino-acid Change
ENST00000381884.9:c.*308_*311delinsAAGT (CENPJ) MANE Select	ENSP00000371308.4:n.*308_*311delinsAAGT
ENST00000616936.4:c.*979_*982delinsAAGT (CENPJ)	ENSP00000477511.1:n.*979_*982delinsAAGT
NM_018451.4:c.*308_*311delinsAAGT (CENPJ)	NP_060921.3:n.*308_*311delinsAAGT
NR_047594.1:n.4637_4640delinsAAGT (CENPJ)
NR_047595.1:n.4435_4438delinsAAGT (CENPJ)
XM_011535156.1:c.*10+3571_*10+3574delinsACTT (RNF17)	XP_011533458.1:n.*10+3571_*10+3574delinsACTT
XM_011535156.2:c.*10+3571_*10+3574delinsACTT (RNF17)	XP_011533458.1:n.*10+3571_*10+3574delinsACTT
NM_018451.5:c.*308_*311delinsAAGT (CENPJ) MANE Select	NP_060921.3:n.*308_*311delinsAAGT
NR_047594.2:n.4609_4612delinsAAGT (CENPJ)
NR_047595.2:n.4407_4410delinsAAGT (CENPJ)