Canonical Allele Identifier: CA473305329

Gene: USH1C

Linked Data

• MyVariant Identifiers: chr11:g.17522662C>G (hg19)

Genomic Alleles

HGVS	Genome Assembly
NC_000011.10:g.17501115C>G , CM000673.2:g.17501115C>G	GRCh38
NC_000011.9:g.17522662C>G , CM000673.1:g.17522662C>G	GRCh37
NC_000011.8:g.17479238C>G	NCBI36
NG_011883.1:g.48302G>C
NG_011883.2:g.48302G>C

Transcript Alleles

HGVS	Amino-acid Change
ENST00000005226.12:c.2316G>C MANE Select	ENSP00000005226.7:p.Val772=
ENST00000318024.9:c.1416G>C MANE Plus Clinical	ENSP00000317018.4:p.Val472=
ENST00000005226.11:c.2316G>C	ENSP00000005226.7:p.Val772=
ENST00000318024.8:c.1416G>C	ENSP00000317018.4:p.Val472=
ENST00000526313.5:c.*130G>C	ENSP00000432236.1:n.*130G>C
ENST00000527020.5:c.1359G>C	ENSP00000436934.1:p.Val453=
ENST00000527720.5:c.1323G>C	ENSP00000432944.1:p.Val441=
ENST00000529563.5:n.300G>C
ENST00000534556.1:n.201G>C
NM_001297764.1:c.1359G>C	NP_001284693.1:p.Val453=
NM_005709.3:c.1416G>C	NP_005700.2:p.Val472=
NM_153676.3:c.2316G>C	NP_710142.1:p.Val772=
NR_123738.1:n.1451G>C
XM_011519831.1:c.2340G>C	XP_011518133.1:p.Val780=
XM_011519832.1:c.1569G>C	XP_011518134.1:p.Val523=
XM_011519833.1:c.*23G>C	XP_011518135.1:n.*23G>C
XR_930841.1:n.1787G>C
XR_930842.1:n.1728G>C
XM_011519832.3:c.1569G>C	XP_011518134.1:p.Val523=
XM_017017075.1:c.2316G>C	XP_016872564.1:p.Val772=
XR_001747717.2:n.1575G>C
NM_153676.4:c.2316G>C MANE Select	NP_710142.1:p.Val772=
NM_001297764.2:c.1359G>C	NP_001284693.1:p.Val453=
NM_005709.4:c.1416G>C MANE Plus Clinical	NP_005700.2:p.Val472=
NR_123738.2:n.1451G>C