Canonical Allele Identifier: CA1955173444

Gene: USH1C

Genomic Alleles

HGVS	Genome Assembly
NC_000011.10:g.17501493G= , CM000673.2:g.17501493G=	GRCh38
NC_000011.9:g.17523040G= , CM000673.1:g.17523040G=	GRCh37
NC_000011.8:g.17479616G=	NCBI36
NG_011883.1:g.47924C=
NG_011883.2:g.47924C=

Transcript Alleles

HGVS	Amino-acid Change
ENST00000005226.12:c.2269C= MANE Select	ENSP00000005226.7:p.Arg757=
ENST00000318024.9:c.1369C= MANE Plus Clinical	ENSP00000317018.4:p.Arg457=
ENST00000005226.11:c.2269C=	ENSP00000005226.7:p.Arg757=
ENST00000318024.8:c.1369C=	ENSP00000317018.4:p.Arg457=
ENST00000526313.5:c.*83C=	ENSP00000432236.1:n.*83C=
ENST00000527020.5:c.1312C=	ENSP00000436934.1:p.Arg438=
ENST00000527720.5:c.1276C=	ENSP00000432944.1:p.Arg426=
ENST00000529563.5:n.253C=
ENST00000534556.1:n.154C=
NM_001297764.1:c.1312C=	NP_001284693.1:p.Arg438=
NM_005709.3:c.1369C=	NP_005700.2:p.Arg457=
NM_153676.3:c.2269C=	NP_710142.1:p.Arg757=
NR_123738.1:n.1404C=
XM_011519831.1:c.2293C=	XP_011518133.1:p.Arg765=
XM_011519832.1:c.1522C=	XP_011518134.1:p.Arg508=
XM_011519833.1:c.1419C=	XP_011518135.1:p.Tyr473=
XR_930841.1:n.1740C=
XR_930842.1:n.1681C=
XM_011519832.3:c.1522C=	XP_011518134.1:p.Arg508=
XM_017017075.1:c.2269C=	XP_016872564.1:p.Arg757=
XR_001747717.2:n.1528C=
NM_153676.4:c.2269C= MANE Select	NP_710142.1:p.Arg757=
NM_001297764.2:c.1312C=	NP_001284693.1:p.Arg438=
NM_005709.4:c.1369C= MANE Plus Clinical	NP_005700.2:p.Arg457=
NR_123738.2:n.1404C=