Canonical Allele Identifier: CA2079394178

Genomic Alleles

HGVS Genome Assembly
NC_000013.11:g.24883252_24883255delinsTTGA , CM000675.2:g.24883252_24883255delinsTTGA GRCh38
NC_000013.10:g.25457390_25457393delinsTTGA , CM000675.1:g.25457390_25457393delinsTTGA GRCh37
NC_000013.9:g.24355390_24355393delinsTTGA NCBI36
NG_009165.2:g.44693_44696delinsTCAA

Transcript Alleles

HGVS Amino-acid change
ENST00000381884.9:c.3939_3942delinsTCAA (CENPJ) MANE Select ENSP00000371308.4:p.His1313=
ENST00000545981.6:c.*679_*682delinsTCAA (CENPJ) ENSP00000441090.2:n.*679_*682delinsTCAA
ENST00000381884.8:c.3939_3942delinsTCAA (CENPJ) ENSP00000371308.4:p.His1313=
ENST00000545981.5:c.*680_*683delinsTCAA (CENPJ) ENSP00000441090.2:n.*680_*683delinsTCAA
ENST00000616936.4:c.*593_*596delinsTCAA (CENPJ) ENSP00000477511.1:n.*593_*596delinsTCAA
NM_018451.4:c.3939_3942delinsTCAA (CENPJ) NP_060921.3:p.His1313=
NR_047594.1:n.4251_4254delinsTCAA (CENPJ)
NR_047595.1:n.4049_4052delinsTCAA (CENPJ)
XM_011535156.1:c.*10+3957_*10+3960delinsTTGA (RNF17) XP_011533458.1:n.*10+3957_*10+3960delinsT...
XM_011535156.2:c.*10+3957_*10+3960delinsTTGA (RNF17) XP_011533458.1:n.*10+3957_*10+3960delinsT...
NM_018451.5:c.3939_3942delinsTCAA (CENPJ) MANE Select NP_060921.3:p.His1313=
NR_047594.2:n.4223_4226delinsTCAA (CENPJ)
NR_047595.2:n.4021_4024delinsTCAA (CENPJ)