Canonical Allele Identifier: CA1998829149

Gene: C11orf65

Genomic Alleles

HGVS	Genome Assembly
NC_000011.10:g.108369259_108369260delinsCG , CM000673.2:g.108369259_108369260delinsCG	GRCh38
NC_000011.9:g.108239986_108239987delinsCG , CM000673.1:g.108239986_108239987delinsCG	GRCh37
NC_000011.8:g.107745196_107745197delinsCG	NCBI36
NG_009830.1:g.151428_151429delinsCG , LRG_135:g.151428_151429delinsCG
NG_054724.1:g.105573_105574delinsCG

Transcript Alleles

HGVS	Amino-acid Change
ENST00000524755.5:c.226+23948_226+23949delinsCG
ENST00000525729.5:c.640+16660_640+16661delinsCG	ENSP00000433395.1:n.640+16660_640+16661delinsCG
ENST00000526725.1:n.271+23948_271+23949delinsCG
ENST00000527531.5:c.*2-13151_*2-13150delinsCG	ENSP00000431706.1:n.*2-13151_*2-13150delinsCG
ENST00000615746.4:c.*2-13151_*2-13150delinsCG	ENSP00000483537.1:n.*2-13151_*2-13150delinsCG
XM_005271414.3:c.787+16660_787+16661delinsCG	XP_005271471.1:n.787+16660_787+16661delinsCG
XM_005271415.3:c.731+23948_731+23949delinsCG	XP_005271472.1:n.731+23948_731+23949delinsCG
XM_011542640.1:c.787+16660_787+16661delinsCG	XP_011540942.1:n.787+16660_787+16661delinsCG
XM_011542642.1:c.732-20187_732-20186delinsCG	XP_011540944.1:n.732-20187_732-20186delinsCG
XM_011542643.1:c.731+23948_731+23949delinsCG	XP_011540945.1:n.731+23948_731+23949delinsCG
NM_001330368.1:c.640+16660_640+16661delinsCG	NP_001317297.1:n.640+16660_640+16661delinsCG
NM_001351110.1:c.694+16660_694+16661delinsCG	NP_001338039.1:n.694+16660_694+16661delinsCG
NR_147053.2:n.1107-13151_1107-13150delinsCG
XM_005271414.4:c.787+16660_787+16661delinsCG	XP_005271471.1:n.787+16660_787+16661delinsCG
XM_005271415.4:c.731+23948_731+23949delinsCG	XP_005271472.1:n.731+23948_731+23949delinsCG
XM_011542640.2:c.787+16660_787+16661delinsCG	XP_011540942.1:n.787+16660_787+16661delinsCG
XM_011542643.2:c.731+23948_731+23949delinsCG	XP_011540945.1:n.731+23948_731+23949delinsCG
XM_017017247.1:c.903+13800_903+13801delinsCG	XP_016872736.1:n.903+13800_903+13801delinsCG
NM_001330368.2:c.640+16660_640+16661delinsCG	NP_001317297.1:n.640+16660_640+16661delinsCG
NM_001351110.2:c.694+16660_694+16661delinsCG	NP_001338039.1:n.694+16660_694+16661delinsCG
NR_147053.3:n.1105-13151_1105-13150delinsCG