Canonical Allele Identifier: CA1998829174
Gene: C11orf65 HGNC NCBI

Linked Data

dbSNP Id: rs2091478237

Genomic Alleles

HGVS Genome Assembly
NC_000011.10:g.108369321_108369324dup , CM000673.2:g.108369321_108369324dup GRCh38
NC_000011.9:g.108240048_108240051dup , CM000673.1:g.108240048_108240051dup GRCh37
NC_000011.8:g.107745258_107745261dup NCBI36
NG_009830.1:g.151490_151493dup , LRG_135:g.151490_151493dup
NG_054724.1:g.105510_105513dup

Transcript Alleles

HGVS Amino-acid Change
ENST00000524755.5:c.226+23885_226+23888dup
ENST00000525729.5:c.640+16597_640+16600dup ENSP00000433395.1:n.640+16597_640+16600dup
ENST00000526725.1:n.271+23885_271+23888dup
ENST00000527531.5:c.*2-13214_*2-13211dup ENSP00000431706.1:n.*2-13214_*2-13211dup
ENST00000615746.4:c.*2-13214_*2-13211dup ENSP00000483537.1:n.*2-13214_*2-13211dup
XM_005271414.3:c.787+16597_787+16600dup XP_005271471.1:n.787+16597_787+16600dup
XM_005271415.3:c.731+23885_731+23888dup XP_005271472.1:n.731+23885_731+23888dup
XM_011542640.1:c.787+16597_787+16600dup XP_011540942.1:n.787+16597_787+16600dup
XM_011542642.1:c.732-20250_732-20247dup XP_011540944.1:n.732-20250_732-20247dup
XM_011542643.1:c.731+23885_731+23888dup XP_011540945.1:n.731+23885_731+23888dup
NM_001330368.1:c.640+16597_640+16600dup NP_001317297.1:n.640+16597_640+16600dup
NM_001351110.1:c.694+16597_694+16600dup NP_001338039.1:n.694+16597_694+16600dup
NR_147053.2:n.1107-13214_1107-13211dup
XM_005271414.4:c.787+16597_787+16600dup XP_005271471.1:n.787+16597_787+16600dup
XM_005271415.4:c.731+23885_731+23888dup XP_005271472.1:n.731+23885_731+23888dup
XM_011542640.2:c.787+16597_787+16600dup XP_011540942.1:n.787+16597_787+16600dup
XM_011542643.2:c.731+23885_731+23888dup XP_011540945.1:n.731+23885_731+23888dup
XM_017017247.1:c.903+13737_903+13740dup XP_016872736.1:n.903+13737_903+13740dup
NM_001330368.2:c.640+16597_640+16600dup NP_001317297.1:n.640+16597_640+16600dup
NM_001351110.2:c.694+16597_694+16600dup NP_001338039.1:n.694+16597_694+16600dup
NR_147053.3:n.1105-13214_1105-13211dup