Canonical Allele Identifier: CA1955173139
Gene: USH1C HGNC NCBI

Genomic Alleles

HGVS Genome Assembly
NC_000011.10:g.17500959C= , CM000673.2:g.17500959C= GRCh38
NC_000011.9:g.17522506C= , CM000673.1:g.17522506C= GRCh37
NC_000011.8:g.17479082C= NCBI36
NG_011883.1:g.48458G=
NG_011883.2:g.48458G=

Transcript Alleles

HGVS Amino-acid change
ENST00000005226.12:c.2380+92G= MANE Select ENSP00000005226.7:n.2380+92G=
ENST00000318024.9:c.1480+92G= MANE Plus Clinical ENSP00000317018.4:n.1480+92G=
ENST00000005226.11:c.2380+92G= ENSP00000005226.7:n.2380+92G=
ENST00000318024.8:c.1480+92G= ENSP00000317018.4:n.1480+92G=
ENST00000526313.5:c.*194+92G= ENSP00000432236.1:n.*194+92G=
ENST00000527020.5:c.1423+92G= ENSP00000436934.1:n.1423+92G=
ENST00000527720.5:c.1387+92G= ENSP00000432944.1:n.1387+92G=
ENST00000529563.5:n.364+92G=
NM_001297764.1:c.1423+92G= NP_001284693.1:n.1423+92G=
NM_005709.3:c.1480+92G= NP_005700.2:n.1480+92G=
NM_153676.3:c.2380+92G= NP_710142.1:n.2380+92G=
NR_123738.1:n.1515+92G=
XM_011519831.1:c.2404+92G= XP_011518133.1:n.2404+92G=
XM_011519832.1:c.1633+92G= XP_011518134.1:n.1633+92G=
XM_011519832.3:c.1633+92G= XP_011518134.1:n.1633+92G=
XM_017017075.1:c.2380+92G= XP_016872564.1:n.2380+92G=
XR_001747717.2:n.1639+92G=
NM_153676.4:c.2380+92G= MANE Select NP_710142.1:n.2380+92G=
NM_001297764.2:c.1423+92G= NP_001284693.1:n.1423+92G=
NM_005709.4:c.1480+92G= MANE Plus Clinical NP_005700.2:n.1480+92G=
NR_123738.2:n.1515+92G=