Canonical Allele Identifier: CA1955173137
Gene: USH1C HGNC NCBI

Genomic Alleles

HGVS Genome Assembly
NC_000011.10:g.17500957_17500958delinsGC , CM000673.2:g.17500957_17500958delinsGC GRCh38
NC_000011.9:g.17522504_17522505delinsGC , CM000673.1:g.17522504_17522505delinsGC GRCh37
NC_000011.8:g.17479080_17479081delinsGC NCBI36
NG_011883.1:g.48459_48460delinsGC
NG_011883.2:g.48459_48460delinsGC

Transcript Alleles

HGVS Amino-acid change
ENST00000005226.12:c.2380+93_2380+94delinsGC MANE Select ENSP00000005226.7:n.2380+93_2380+94delins...
ENST00000318024.9:c.1480+93_1480+94delinsGC MANE Plus Clinical ENSP00000317018.4:n.1480+93_1480+94delins...
ENST00000005226.11:c.2380+93_2380+94delinsGC ENSP00000005226.7:n.2380+93_2380+94delins...
ENST00000318024.8:c.1480+93_1480+94delinsGC ENSP00000317018.4:n.1480+93_1480+94delins...
ENST00000526313.5:c.*194+93_*194+94delinsGC ENSP00000432236.1:n.*194+93_*194+94delins...
ENST00000527020.5:c.1423+93_1423+94delinsGC ENSP00000436934.1:n.1423+93_1423+94delins...
ENST00000527720.5:c.1387+93_1387+94delinsGC ENSP00000432944.1:n.1387+93_1387+94delins...
ENST00000529563.5:n.364+93_364+94delinsGC
NM_001297764.1:c.1423+93_1423+94delinsGC NP_001284693.1:n.1423+93_1423+94delinsGC
NM_005709.3:c.1480+93_1480+94delinsGC NP_005700.2:n.1480+93_1480+94delinsGC
NM_153676.3:c.2380+93_2380+94delinsGC NP_710142.1:n.2380+93_2380+94delinsGC
NR_123738.1:n.1515+93_1515+94delinsGC
XM_011519831.1:c.2404+93_2404+94delinsGC XP_011518133.1:n.2404+93_2404+94delinsGC
XM_011519832.1:c.1633+93_1633+94delinsGC XP_011518134.1:n.1633+93_1633+94delinsGC
XM_011519832.3:c.1633+93_1633+94delinsGC XP_011518134.1:n.1633+93_1633+94delinsGC
XM_017017075.1:c.2380+93_2380+94delinsGC XP_016872564.1:n.2380+93_2380+94delinsGC
XR_001747717.2:n.1639+93_1639+94delinsGC
NM_153676.4:c.2380+93_2380+94delinsGC MANE Select NP_710142.1:n.2380+93_2380+94delinsGC
NM_001297764.2:c.1423+93_1423+94delinsGC NP_001284693.1:n.1423+93_1423+94delinsGC
NM_005709.4:c.1480+93_1480+94delinsGC MANE Plus Clinical NP_005700.2:n.1480+93_1480+94delinsGC
NR_123738.2:n.1515+93_1515+94delinsGC