Canonical Allele Identifier: CA671420079
Gene: C11orf65 HGNC NCBI

Linked Data

dbSNP Id: rs1489728140

Genomic Alleles

HGVS Genome Assembly
NC_000011.10:g.108412490_108412495del , CM000673.2:g.108412490_108412495del GRCh38
NC_000011.9:g.108283217_108283222del , CM000673.1:g.108283217_108283222del GRCh37
NC_000011.8:g.107788427_107788432del NCBI36
NG_054724.1:g.62339_62344del

Transcript Alleles

HGVS Amino-acid change
ENST00000393084.6:c.175-5345_175-5340del MANE Select ENSP00000376799.1:n.175-5345_175-5340del
ENST00000393084.5:c.175-5345_175-5340del ENSP00000376799.1:n.175-5345_175-5340del
ENST00000525729.5:c.82-5531_82-5526del ENSP00000433395.1:n.82-5531_82-5526del
ENST00000527531.5:c.175-5345_175-5340del ENSP00000431706.1:n.175-5345_175-5340del
ENST00000529391.5:c.175-5345_175-5340del ENSP00000436400.1:n.175-5345_175-5340del
ENST00000533583.1:c.175-5531_175-5526del ENSP00000434500.1:n.175-5531_175-5526del
ENST00000615746.4:c.175-5345_175-5340del ENSP00000483537.1:n.175-5345_175-5340del
NM_152587.3:c.175-5345_175-5340del NP_689800.3:n.175-5345_175-5340del
XM_005271412.2:c.175-5531_175-5526del XP_005271469.1:n.175-5531_175-5526del
XM_005271413.2:c.82-5345_82-5340del XP_005271470.1:n.82-5345_82-5340del
XM_005271414.3:c.175-5345_175-5340del XP_005271471.1:n.175-5345_175-5340del
XM_005271415.3:c.175-5345_175-5340del XP_005271472.1:n.175-5345_175-5340del
XM_011542639.1:c.175-5345_175-5340del XP_011540941.1:n.175-5345_175-5340del
XM_011542640.1:c.175-5345_175-5340del XP_011540942.1:n.175-5345_175-5340del
XM_011542641.1:c.82-5531_82-5526del XP_011540943.1:n.82-5531_82-5526del
XM_011542642.1:c.175-5345_175-5340del XP_011540944.1:n.175-5345_175-5340del
XM_011542643.1:c.175-5345_175-5340del XP_011540945.1:n.175-5345_175-5340del
NM_001330368.1:c.82-5531_82-5526del NP_001317297.1:n.82-5531_82-5526del
NM_001351110.1:c.82-5345_82-5340del NP_001338039.1:n.82-5345_82-5340del
NM_152587.4:c.175-5345_175-5340del NP_689800.3:n.175-5345_175-5340del
NR_147053.2:n.338-5345_338-5340del
XM_005271412.3:c.175-5531_175-5526del XP_005271469.1:n.175-5531_175-5526del
XM_005271413.3:c.82-5345_82-5340del XP_005271470.1:n.82-5345_82-5340del
XM_005271414.4:c.175-5345_175-5340del XP_005271471.1:n.175-5345_175-5340del
XM_005271415.4:c.175-5345_175-5340del XP_005271472.1:n.175-5345_175-5340del
XM_011542639.2:c.175-5345_175-5340del XP_011540941.1:n.175-5345_175-5340del
XM_011542640.2:c.175-5345_175-5340del XP_011540942.1:n.175-5345_175-5340del
XM_011542641.2:c.82-5531_82-5526del XP_011540943.1:n.82-5531_82-5526del
XM_011542643.2:c.175-5345_175-5340del XP_011540945.1:n.175-5345_175-5340del
XM_017017246.1:c.175-5345_175-5340del XP_016872735.1:n.175-5345_175-5340del
XM_017017247.1:c.175-5345_175-5340del XP_016872736.1:n.175-5345_175-5340del
XM_017017248.1:c.175-5345_175-5340del XP_016872737.1:n.175-5345_175-5340del
NM_152587.5:c.175-5345_175-5340del MANE Select NP_689800.3:n.175-5345_175-5340del
NM_001330368.2:c.82-5531_82-5526del NP_001317297.1:n.82-5531_82-5526del
NM_001351110.2:c.82-5345_82-5340del NP_001338039.1:n.82-5345_82-5340del
NR_147053.3:n.336-5345_336-5340del