Canonical Allele Identifier: CA1955186867
Gene: USH1C HGNC NCBI

Genomic Alleles

HGVS Genome Assembly
NC_000011.10:g.17527017T= , CM000673.2:g.17527017T= GRCh38
NC_000011.9:g.17548564T= , CM000673.1:g.17548564T= GRCh37
NC_000011.8:g.17505140T= NCBI36
NG_011883.1:g.22400A=
NG_011883.2:g.22400A=

Transcript Alleles

HGVS Amino-acid Change
ENST00000005226.12:c.520A= MANE Select ENSP00000005226.7:p.Ser174=
ENST00000318024.9:c.520A= MANE Plus Clinical ENSP00000317018.4:p.Ser174=
ENST00000005226.11:c.520A= ENSP00000005226.7:p.Ser174=
ENST00000318024.8:c.520A= ENSP00000317018.4:p.Ser174=
ENST00000526181.1:c.553A= ENSP00000437128.1:p.Ser185=
ENST00000526313.5:c.520A= ENSP00000432236.1:p.Ser174=
ENST00000527020.5:c.520A= ENSP00000436934.1:p.Ser174=
ENST00000527720.5:c.427A= ENSP00000432944.1:p.Ser143=
NM_001297764.1:c.520A= NP_001284693.1:p.Ser174=
NM_005709.3:c.520A= NP_005700.2:p.Ser174=
NM_153676.3:c.520A= NP_710142.1:p.Ser174=
NR_123738.1:n.629A=
XM_011519831.1:c.520A= XP_011518133.1:p.Ser174=
XM_011519832.1:c.520A= XP_011518134.1:p.Ser174=
XM_011519833.1:c.520A= XP_011518135.1:p.Ser174=
XM_011519834.1:c.520A= XP_011518136.1:p.Ser174=
XR_930841.1:n.629A=
XR_930842.1:n.629A=
XM_011519832.3:c.520A= XP_011518134.1:p.Ser174=
XM_011519834.2:c.520A= XP_011518136.1:p.Ser174=
XM_017017072.1:c.520A= XP_016872561.1:p.Ser174=
XM_017017073.1:c.520A= XP_016872562.1:p.Ser174=
XM_017017074.1:c.520A= XP_016872563.1:p.Ser174=
XM_017017075.1:c.520A= XP_016872564.1:p.Ser174=
XR_001747717.2:n.629A=
NM_153676.4:c.520A= MANE Select NP_710142.1:p.Ser174=
NM_001297764.2:c.520A= NP_001284693.1:p.Ser174=
NM_005709.4:c.520A= MANE Plus Clinical NP_005700.2:p.Ser174=
NR_123738.2:n.629A=