Canonical Allele Identifier: CA2079393947

Genomic Alleles

HGVS Genome Assembly
NC_000013.11:g.24882869_24882873delinsTCTTG , CM000675.2:g.24882869_24882873delinsTCTTG GRCh38
NC_000013.10:g.25457007_25457011delinsTCTTG , CM000675.1:g.25457007_25457011delinsTCTTG GRCh37
NC_000013.9:g.24355007_24355011delinsTCTTG NCBI36
NG_009165.2:g.45075_45079delinsCAAGA

Transcript Alleles

HGVS Amino-acid Change
ENST00000381884.9:c.*304_*308delinsCAAGA (CENPJ) MANE Select ENSP00000371308.4:n.*304_*308delinsCAAGA
ENST00000616936.4:c.*975_*979delinsCAAGA (CENPJ) ENSP00000477511.1:n.*975_*979delinsCAAGA
NM_018451.4:c.*304_*308delinsCAAGA (CENPJ) NP_060921.3:n.*304_*308delinsCAAGA
NR_047594.1:n.4633_4637delinsCAAGA (CENPJ)
NR_047595.1:n.4431_4435delinsCAAGA (CENPJ)
XM_011535156.1:c.*10+3574_*10+3578delinsTCTTG (RNF17) XP_011533458.1:n.*10+3574_*10+3578delinsTCTTG
XM_011535156.2:c.*10+3574_*10+3578delinsTCTTG (RNF17) XP_011533458.1:n.*10+3574_*10+3578delinsTCTTG
NM_018451.5:c.*304_*308delinsCAAGA (CENPJ) MANE Select NP_060921.3:n.*304_*308delinsCAAGA
NR_047594.2:n.4605_4609delinsCAAGA (CENPJ)
NR_047595.2:n.4403_4407delinsCAAGA (CENPJ)