Canonical Allele Identifier: CA942024846
Gene: C11orf65 HGNC NCBI

Linked Data

Genomic Alleles

HGVS Genome Assembly
NC_000011.10:g.108369331_108369342del , CM000673.2:g.108369331_108369342del GRCh38
NC_000011.9:g.108240058_108240069del , CM000673.1:g.108240058_108240069del GRCh37
NC_000011.8:g.107745268_107745279del NCBI36
NG_009830.1:g.151500_151511del , LRG_135:g.151500_151511del
NG_054724.1:g.105491_105502del

Transcript Alleles

HGVS Amino-acid Change
ENST00000524755.5:c.226+23866_226+23877del
ENST00000525729.5:c.640+16578_640+16589del ENSP00000433395.1:n.640+16578_640+16589del
ENST00000526725.1:n.271+23866_271+23877del
ENST00000527531.5:c.*2-13233_*2-13222del ENSP00000431706.1:n.*2-13233_*2-13222del
ENST00000615746.4:c.*2-13233_*2-13222del ENSP00000483537.1:n.*2-13233_*2-13222del
XM_005271414.3:c.787+16578_787+16589del XP_005271471.1:n.787+16578_787+16589del
XM_005271415.3:c.731+23866_731+23877del XP_005271472.1:n.731+23866_731+23877del
XM_011542640.1:c.787+16578_787+16589del XP_011540942.1:n.787+16578_787+16589del
XM_011542642.1:c.732-20269_732-20258del XP_011540944.1:n.732-20269_732-20258del
XM_011542643.1:c.731+23866_731+23877del XP_011540945.1:n.731+23866_731+23877del
NM_001330368.1:c.640+16578_640+16589del NP_001317297.1:n.640+16578_640+16589del
NM_001351110.1:c.694+16578_694+16589del NP_001338039.1:n.694+16578_694+16589del
NR_147053.2:n.1107-13233_1107-13222del
XM_005271414.4:c.787+16578_787+16589del XP_005271471.1:n.787+16578_787+16589del
XM_005271415.4:c.731+23866_731+23877del XP_005271472.1:n.731+23866_731+23877del
XM_011542640.2:c.787+16578_787+16589del XP_011540942.1:n.787+16578_787+16589del
XM_011542643.2:c.731+23866_731+23877del XP_011540945.1:n.731+23866_731+23877del
XM_017017247.1:c.903+13718_903+13729del XP_016872736.1:n.903+13718_903+13729del
NM_001330368.2:c.640+16578_640+16589del NP_001317297.1:n.640+16578_640+16589del
NM_001351110.2:c.694+16578_694+16589del NP_001338039.1:n.694+16578_694+16589del
NR_147053.3:n.1105-13233_1105-13222del