Canonical Allele Identifier: CA671419982

Gene: C11orf65

Linked Data

• dbSNP Id: rs1221655649
• gnomAD v3: 11-108412327-CAACA-C
• gnomAD v4: 11-108412327-CAACA-C
• MyVariant Identifiers: chr11:g.108283055_108283058del (hg19) ; chr11:g.108412328_108412331del (hg38)

Genomic Alleles

HGVS	Genome Assembly
NC_000011.10:g.108412332_108412335del , CM000673.2:g.108412332_108412335del	GRCh38
NC_000011.9:g.108283059_108283062del , CM000673.1:g.108283059_108283062del	GRCh37
NC_000011.8:g.107788269_107788272del	NCBI36
NG_054724.1:g.62502_62505del

Transcript Alleles

HGVS	Amino-acid change
ENST00000393084.6:c.175-5182_175-5179del MANE Select	ENSP00000376799.1:n.175-5182_175-5179del
ENST00000393084.5:c.175-5182_175-5179del	ENSP00000376799.1:n.175-5182_175-5179del
ENST00000525729.5:c.82-5368_82-5365del	ENSP00000433395.1:n.82-5368_82-5365del
ENST00000527531.5:c.175-5182_175-5179del	ENSP00000431706.1:n.175-5182_175-5179del
ENST00000529391.5:c.175-5182_175-5179del	ENSP00000436400.1:n.175-5182_175-5179del
ENST00000533583.1:c.175-5368_175-5365del	ENSP00000434500.1:n.175-5368_175-5365del
ENST00000615746.4:c.175-5182_175-5179del	ENSP00000483537.1:n.175-5182_175-5179del
NM_152587.3:c.175-5182_175-5179del	NP_689800.3:n.175-5182_175-5179del
XM_005271412.2:c.175-5368_175-5365del	XP_005271469.1:n.175-5368_175-5365del
XM_005271413.2:c.82-5182_82-5179del	XP_005271470.1:n.82-5182_82-5179del
XM_005271414.3:c.175-5182_175-5179del	XP_005271471.1:n.175-5182_175-5179del
XM_005271415.3:c.175-5182_175-5179del	XP_005271472.1:n.175-5182_175-5179del
XM_011542639.1:c.175-5182_175-5179del	XP_011540941.1:n.175-5182_175-5179del
XM_011542640.1:c.175-5182_175-5179del	XP_011540942.1:n.175-5182_175-5179del
XM_011542641.1:c.82-5368_82-5365del	XP_011540943.1:n.82-5368_82-5365del
XM_011542642.1:c.175-5182_175-5179del	XP_011540944.1:n.175-5182_175-5179del
XM_011542643.1:c.175-5182_175-5179del	XP_011540945.1:n.175-5182_175-5179del
NM_001330368.1:c.82-5368_82-5365del	NP_001317297.1:n.82-5368_82-5365del
NM_001351110.1:c.82-5182_82-5179del	NP_001338039.1:n.82-5182_82-5179del
NM_152587.4:c.175-5182_175-5179del	NP_689800.3:n.175-5182_175-5179del
NR_147053.2:n.338-5182_338-5179del
XM_005271412.3:c.175-5368_175-5365del	XP_005271469.1:n.175-5368_175-5365del
XM_005271413.3:c.82-5182_82-5179del	XP_005271470.1:n.82-5182_82-5179del
XM_005271414.4:c.175-5182_175-5179del	XP_005271471.1:n.175-5182_175-5179del
XM_005271415.4:c.175-5182_175-5179del	XP_005271472.1:n.175-5182_175-5179del
XM_011542639.2:c.175-5182_175-5179del	XP_011540941.1:n.175-5182_175-5179del
XM_011542640.2:c.175-5182_175-5179del	XP_011540942.1:n.175-5182_175-5179del
XM_011542641.2:c.82-5368_82-5365del	XP_011540943.1:n.82-5368_82-5365del
XM_011542643.2:c.175-5182_175-5179del	XP_011540945.1:n.175-5182_175-5179del
XM_017017246.1:c.175-5182_175-5179del	XP_016872735.1:n.175-5182_175-5179del
XM_017017247.1:c.175-5182_175-5179del	XP_016872736.1:n.175-5182_175-5179del
XM_017017248.1:c.175-5182_175-5179del	XP_016872737.1:n.175-5182_175-5179del
NM_152587.5:c.175-5182_175-5179del MANE Select	NP_689800.3:n.175-5182_175-5179del
NM_001330368.2:c.82-5368_82-5365del	NP_001317297.1:n.82-5368_82-5365del
NM_001351110.2:c.82-5182_82-5179del	NP_001338039.1:n.82-5182_82-5179del
NR_147053.3:n.336-5182_336-5179del