Canonical Allele Identifier: CA228372378

Gene: C11orf65

Linked Data

• dbSNP Id: rs1001221668
• gnomAD v3: 11-108412328-AACAAACAGGAAACAATTACAAAT-A
• gnomAD v4: 11-108412328-AACAAACAGGAAACAATTACAAAT-A
• MyVariant Identifiers: chr11:g.108283056_108283078del (hg19) ; chr11:g.108412329_108412351del (hg38)

Genomic Alleles

HGVS	Genome Assembly
NC_000011.10:g.108412333_108412355del , CM000673.2:g.108412333_108412355del	GRCh38
NC_000011.9:g.108283060_108283082del , CM000673.1:g.108283060_108283082del	GRCh37
NC_000011.8:g.107788270_107788292del	NCBI36
NG_054724.1:g.62482_62504del

Transcript Alleles

HGVS	Amino-acid change
ENST00000393084.6:c.175-5202_175-5180del MANE Select	ENSP00000376799.1:n.175-5202_175-5180del
ENST00000393084.5:c.175-5202_175-5180del	ENSP00000376799.1:n.175-5202_175-5180del
ENST00000525729.5:c.82-5388_82-5366del	ENSP00000433395.1:n.82-5388_82-5366del
ENST00000527531.5:c.175-5202_175-5180del	ENSP00000431706.1:n.175-5202_175-5180del
ENST00000529391.5:c.175-5202_175-5180del	ENSP00000436400.1:n.175-5202_175-5180del
ENST00000533583.1:c.175-5388_175-5366del	ENSP00000434500.1:n.175-5388_175-5366del
ENST00000615746.4:c.175-5202_175-5180del	ENSP00000483537.1:n.175-5202_175-5180del
NM_152587.3:c.175-5202_175-5180del	NP_689800.3:n.175-5202_175-5180del
XM_005271412.2:c.175-5388_175-5366del	XP_005271469.1:n.175-5388_175-5366del
XM_005271413.2:c.82-5202_82-5180del	XP_005271470.1:n.82-5202_82-5180del
XM_005271414.3:c.175-5202_175-5180del	XP_005271471.1:n.175-5202_175-5180del
XM_005271415.3:c.175-5202_175-5180del	XP_005271472.1:n.175-5202_175-5180del
XM_011542639.1:c.175-5202_175-5180del	XP_011540941.1:n.175-5202_175-5180del
XM_011542640.1:c.175-5202_175-5180del	XP_011540942.1:n.175-5202_175-5180del
XM_011542641.1:c.82-5388_82-5366del	XP_011540943.1:n.82-5388_82-5366del
XM_011542642.1:c.175-5202_175-5180del	XP_011540944.1:n.175-5202_175-5180del
XM_011542643.1:c.175-5202_175-5180del	XP_011540945.1:n.175-5202_175-5180del
NM_001330368.1:c.82-5388_82-5366del	NP_001317297.1:n.82-5388_82-5366del
NM_001351110.1:c.82-5202_82-5180del	NP_001338039.1:n.82-5202_82-5180del
NM_152587.4:c.175-5202_175-5180del	NP_689800.3:n.175-5202_175-5180del
NR_147053.2:n.338-5202_338-5180del
XM_005271412.3:c.175-5388_175-5366del	XP_005271469.1:n.175-5388_175-5366del
XM_005271413.3:c.82-5202_82-5180del	XP_005271470.1:n.82-5202_82-5180del
XM_005271414.4:c.175-5202_175-5180del	XP_005271471.1:n.175-5202_175-5180del
XM_005271415.4:c.175-5202_175-5180del	XP_005271472.1:n.175-5202_175-5180del
XM_011542639.2:c.175-5202_175-5180del	XP_011540941.1:n.175-5202_175-5180del
XM_011542640.2:c.175-5202_175-5180del	XP_011540942.1:n.175-5202_175-5180del
XM_011542641.2:c.82-5388_82-5366del	XP_011540943.1:n.82-5388_82-5366del
XM_011542643.2:c.175-5202_175-5180del	XP_011540945.1:n.175-5202_175-5180del
XM_017017246.1:c.175-5202_175-5180del	XP_016872735.1:n.175-5202_175-5180del
XM_017017247.1:c.175-5202_175-5180del	XP_016872736.1:n.175-5202_175-5180del
XM_017017248.1:c.175-5202_175-5180del	XP_016872737.1:n.175-5202_175-5180del
NM_152587.5:c.175-5202_175-5180del MANE Select	NP_689800.3:n.175-5202_175-5180del
NM_001330368.2:c.82-5388_82-5366del	NP_001317297.1:n.82-5388_82-5366del
NM_001351110.2:c.82-5202_82-5180del	NP_001338039.1:n.82-5202_82-5180del
NR_147053.3:n.336-5202_336-5180del