Canonical Allele Identifier: CA1955171725
Gene: USH1C HGNC NCBI

Genomic Alleles

HGVS Genome Assembly
NC_000011.10:g.17498216G= , CM000673.2:g.17498216G= GRCh38
NC_000011.9:g.17519763G= , CM000673.1:g.17519763G= GRCh37
NC_000011.8:g.17476339G= NCBI36
NG_011883.1:g.51201C=
NG_011883.2:g.51201C=

Transcript Alleles

HGVS Amino-acid change
ENST00000005226.12:c.2436C= MANE Select ENSP00000005226.7:p.Asp812=
ENST00000318024.9:c.1536C= MANE Plus Clinical ENSP00000317018.4:p.Asp512=
ENST00000005226.11:c.2436C= ENSP00000005226.7:p.Asp812=
ENST00000318024.8:c.1536C= ENSP00000317018.4:p.Asp512=
ENST00000526313.5:c.*250C= ENSP00000432236.1:n.*250C=
ENST00000527020.5:c.1479C= ENSP00000436934.1:p.Asp493=
ENST00000527720.5:c.1443C= ENSP00000432944.1:p.Asp481=
ENST00000529563.5:n.420C=
NM_001297764.1:c.1479C= NP_001284693.1:p.Asp493=
NM_005709.3:c.1536C= NP_005700.2:p.Asp512=
NM_153676.3:c.2436C= NP_710142.1:p.Asp812=
NR_123738.1:n.1571C=
XM_011519831.1:c.2460C= XP_011518133.1:p.Asp820=
XM_011519832.1:c.1689C= XP_011518134.1:p.Asp563=
XM_011519832.3:c.1689C= XP_011518134.1:p.Asp563=
XM_017017075.1:c.2436C= XP_016872564.1:p.Asp812=
XR_001747717.2:n.1695C=
NM_153676.4:c.2436C= MANE Select NP_710142.1:p.Asp812=
NM_001297764.2:c.1479C= NP_001284693.1:p.Asp493=
NM_005709.4:c.1536C= MANE Plus Clinical NP_005700.2:p.Asp512=
NR_123738.2:n.1571C=