Canonical Allele Identifier: CA2612677170
Gene: USH1C HGNC NCBI

Linked Data

Genomic Alleles

HGVS Genome Assembly
NC_000011.10:g.17527209_17527210insCCCCGCCCTCCCTCCCTCCCACCGTCATGGAGTACGGCCCTGCTC , CM000673.2:g.17527209_17527210insCCCCGCCCTCCCTCCCTCCCACCGTCATGGAGTACGGCCCTGCTC GRCh38
NC_000011.9:g.17548756_17548757insCCCCGCCCTCCCTCCCTCCCACCGTCATGGAGTACGGCCCTGCTC , CM000673.1:g.17548756_17548757insCCCCGCCCTCCCTCCCTCCCACCGTCATGGAGTACGGCCCTGCTC GRCh37
NC_000011.8:g.17505332_17505333insCCCCGCCCTCCCTCCCTCCCACCGTCATGGAGTACGGCCCTGCTC NCBI36
NG_011883.1:g.22216_22217insCGTACTCCATGACGGTGGGAGGGAGGGAGGGCGGGGGAGCAGGGC
NG_011883.2:g.22216_22217insCGTACTCCATGACGGTGGGAGGGAGGGAGGGCGGGGGAGCAGGGC

Transcript Alleles

HGVS Amino-acid Change
ENST00000005226.12:c.496+22_496+23insCGTACTCCATGACGGTGGGAGGGAGGGAGGGCGGGGGAGCAGGGC MANE Select ENSP00000005226.7:n.496+22_496+23insCGTACTCCATGACGGTGGGAGGGAG...
ENST00000318024.9:c.496+22_496+23insCGTACTCCATGACGGTGGGAGGGAGGGAGGGCGGGGGAGCAGGGC MANE Plus Clinical ENSP00000317018.4:n.496+22_496+23insCGTACTCCATGACGGTGGGAGGGAG...
ENST00000005226.11:c.496+22_496+23insCGTACTCCATGACGGTGGGAGGGAGGGAGGGCGGGGGAGCAGGGC ENSP00000005226.7:n.496+22_496+23insCGTACTCCATGACGGTGGGAGGGAG...
ENST00000318024.8:c.496+22_496+23insCGTACTCCATGACGGTGGGAGGGAGGGAGGGCGGGGGAGCAGGGC ENSP00000317018.4:n.496+22_496+23insCGTACTCCATGACGGTGGGAGGGAG...
ENST00000526181.1:c.529+22_529+23insCGTACTCCATGACGGTGGGAGGGAGGGAGGGCGGGGGAGCAGGGC ENSP00000437128.1:n.529+22_529+23insCGTACTCCATGACGGTGGGAGGGAG...
ENST00000526313.5:c.496+22_496+23insCGTACTCCATGACGGTGGGAGGGAGGGAGGGCGGGGGAGCAGGGC ENSP00000432236.1:n.496+22_496+23insCGTACTCCATGACGGTGGGAGGGAG...
ENST00000527020.5:c.496+22_496+23insCGTACTCCATGACGGTGGGAGGGAGGGAGGGCGGGGGAGCAGGGC ENSP00000436934.1:n.496+22_496+23insCGTACTCCATGACGGTGGGAGGGAG...
ENST00000527720.5:c.403+22_403+23insCGTACTCCATGACGGTGGGAGGGAGGGAGGGCGGGGGAGCAGGGC ENSP00000432944.1:n.403+22_403+23insCGTACTCCATGACGGTGGGAGGGAG...
NM_001297764.1:c.496+22_496+23insCGTACTCCATGACGGTGGGAGGGAGGGAGGGCGGGGGAGCAGGGC NP_001284693.1:n.496+22_496+23insCGTACTCCATGACGGTGGGAGGGAGGGA...
NM_005709.3:c.496+22_496+23insCGTACTCCATGACGGTGGGAGGGAGGGAGGGCGGGGGAGCAGGGC NP_005700.2:n.496+22_496+23insCGTACTCCATGACGGTGGGAGGGAGGGAGGG...
NM_153676.3:c.496+22_496+23insCGTACTCCATGACGGTGGGAGGGAGGGAGGGCGGGGGAGCAGGGC NP_710142.1:n.496+22_496+23insCGTACTCCATGACGGTGGGAGGGAGGGAGGG...
NR_123738.1:n.605+22_605+23insCGTACTCCATGACGGTGGGAGGGAGGGAGGGCGGGGGAGCAGGGC
XM_011519831.1:c.496+22_496+23insCGTACTCCATGACGGTGGGAGGGAGGGAGGGCGGGGGAGCAGGGC XP_011518133.1:n.496+22_496+23insCGTACTCCATGACGGTGGGAGGGAGGGA...
XM_011519832.1:c.496+22_496+23insCGTACTCCATGACGGTGGGAGGGAGGGAGGGCGGGGGAGCAGGGC XP_011518134.1:n.496+22_496+23insCGTACTCCATGACGGTGGGAGGGAGGGA...
XM_011519833.1:c.496+22_496+23insCGTACTCCATGACGGTGGGAGGGAGGGAGGGCGGGGGAGCAGGGC XP_011518135.1:n.496+22_496+23insCGTACTCCATGACGGTGGGAGGGAGGGA...
XM_011519834.1:c.496+22_496+23insCGTACTCCATGACGGTGGGAGGGAGGGAGGGCGGGGGAGCAGGGC XP_011518136.1:n.496+22_496+23insCGTACTCCATGACGGTGGGAGGGAGGGA...
XR_930841.1:n.605+22_605+23insCGTACTCCATGACGGTGGGAGGGAGGGAGGGCGGGGGAGCAGGGC
XR_930842.1:n.605+22_605+23insCGTACTCCATGACGGTGGGAGGGAGGGAGGGCGGGGGAGCAGGGC
XM_011519832.3:c.496+22_496+23insCGTACTCCATGACGGTGGGAGGGAGGGAGGGCGGGGGAGCAGGGC XP_011518134.1:n.496+22_496+23insCGTACTCCATGACGGTGGGAGGGAGGGA...
XM_011519834.2:c.496+22_496+23insCGTACTCCATGACGGTGGGAGGGAGGGAGGGCGGGGGAGCAGGGC XP_011518136.1:n.496+22_496+23insCGTACTCCATGACGGTGGGAGGGAGGGA...
XM_017017072.1:c.496+22_496+23insCGTACTCCATGACGGTGGGAGGGAGGGAGGGCGGGGGAGCAGGGC XP_016872561.1:n.496+22_496+23insCGTACTCCATGACGGTGGGAGGGAGGGA...
XM_017017073.1:c.496+22_496+23insCGTACTCCATGACGGTGGGAGGGAGGGAGGGCGGGGGAGCAGGGC XP_016872562.1:n.496+22_496+23insCGTACTCCATGACGGTGGGAGGGAGGGA...
XM_017017074.1:c.496+22_496+23insCGTACTCCATGACGGTGGGAGGGAGGGAGGGCGGGGGAGCAGGGC XP_016872563.1:n.496+22_496+23insCGTACTCCATGACGGTGGGAGGGAGGGA...
XM_017017075.1:c.496+22_496+23insCGTACTCCATGACGGTGGGAGGGAGGGAGGGCGGGGGAGCAGGGC XP_016872564.1:n.496+22_496+23insCGTACTCCATGACGGTGGGAGGGAGGGA...
XR_001747717.2:n.605+22_605+23insCGTACTCCATGACGGTGGGAGGGAGGGAGGGCGGGGGAGCAGGGC
NM_153676.4:c.496+22_496+23insCGTACTCCATGACGGTGGGAGGGAGGGAGGGCGGGGGAGCAGGGC MANE Select NP_710142.1:n.496+22_496+23insCGTACTCCATGACGGTGGGAGGGAGGGAGGG...
NM_001297764.2:c.496+22_496+23insCGTACTCCATGACGGTGGGAGGGAGGGAGGGCGGGGGAGCAGGGC NP_001284693.1:n.496+22_496+23insCGTACTCCATGACGGTGGGAGGGAGGGA...
NM_005709.4:c.496+22_496+23insCGTACTCCATGACGGTGGGAGGGAGGGAGGGCGGGGGAGCAGGGC MANE Plus Clinical NP_005700.2:n.496+22_496+23insCGTACTCCATGACGGTGGGAGGGAGGGAGGG...
NR_123738.2:n.605+22_605+23insCGTACTCCATGACGGTGGGAGGGAGGGAGGGCGGGGGAGCAGGGC