Canonical Allele Identifier: CA142318
Gene: USH1C HGNC NCBI

Linked Data

ClinVar Variation Id: 47988
ClinVar RCV Id: RCV000041264
dbSNP Id: rs397517873

Genomic Alleles

HGVS Genome Assembly
NC_000011.10:g.17505916G>A , CM000673.2:g.17505916G>A GRCh38
NC_000011.9:g.17527463G>A , CM000673.1:g.17527463G>A GRCh37
NC_000011.8:g.17484039G>A NCBI36
NG_011883.1:g.43501C>T
NG_011883.2:g.43501C>T

Transcript Alleles

HGVS Amino-acid change
ENST00000005226.12:c.2047C>T MANE Select ENSP00000005226.7:p.Pro683Ser
ENST00000318024.9:c.1285-3936C>T MANE Plus Clinical ENSP00000317018.4:n.1285-3936C>T
ENST00000005226.11:c.2047C>T ENSP00000005226.7:p.Pro683Ser
ENST00000318024.8:c.1285-3936C>T ENSP00000317018.4:n.1285-3936C>T
ENST00000526313.5:c.1211-3936C>T ENSP00000432236.1:n.1211-3936C>T
ENST00000527020.5:c.1228-3936C>T ENSP00000436934.1:n.1228-3936C>T
ENST00000527720.5:c.1192-3936C>T ENSP00000432944.1:n.1192-3936C>T
ENST00000529563.5:n.169-3936C>T
NM_001297764.1:c.1228-3936C>T NP_001284693.1:n.1228-3936C>T
NM_005709.3:c.1285-3936C>T NP_005700.2:n.1285-3936C>T
NM_153676.3:c.2047C>T NP_710142.1:p.Pro683Ser
NR_123738.1:n.1320-3936C>T
XM_011519831.1:c.2071C>T XP_011518133.1:p.Pro691Ser
XM_011519832.1:c.1438-3936C>T XP_011518134.1:n.1438-3936C>T
XM_011519833.1:c.1335-3936C>T XP_011518135.1:n.1335-3936C>T
XR_930841.1:n.1656-3936C>T
XR_930842.1:n.1597-3936C>T
XM_011519832.3:c.1438-3936C>T XP_011518134.1:n.1438-3936C>T
XM_017017072.1:c.*3206C>T XP_016872561.1:n.*3206C>T
XM_017017073.1:c.*3206C>T XP_016872562.1:n.*3206C>T
XM_017017074.1:c.*3206C>T XP_016872563.1:n.*3206C>T
XM_017017075.1:c.2047C>T XP_016872564.1:p.Pro683Ser
XR_001747717.2:n.1444-3936C>T
NM_153676.4:c.2047C>T MANE Select NP_710142.1:p.Pro683Ser
NM_001297764.2:c.1228-3936C>T NP_001284693.1:n.1228-3936C>T
NM_005709.4:c.1285-3936C>T MANE Plus Clinical NP_005700.2:n.1285-3936C>T
NR_123738.2:n.1320-3936C>T