Canonical Allele Identifier: CA379803238

Gene: USH1C

Linked Data

• MyVariant Identifiers: chr11:g.17522696T>G (hg19) ; chr11:g.17501149T>G (hg38)

Genomic Alleles

HGVS	Genome Assembly
NC_000011.10:g.17501149T>G , CM000673.2:g.17501149T>G	GRCh38
NC_000011.9:g.17522696T>G , CM000673.1:g.17522696T>G	GRCh37
NC_000011.8:g.17479272T>G	NCBI36
NG_011883.1:g.48268A>C
NG_011883.2:g.48268A>C

Transcript Alleles

HGVS	Amino-acid Change
ENST00000005226.12:c.2282A>C MANE Select	ENSP00000005226.7:p.Glu761Ala
ENST00000318024.9:c.1382A>C MANE Plus Clinical	ENSP00000317018.4:p.Glu461Ala
ENST00000005226.11:c.2282A>C	ENSP00000005226.7:p.Glu761Ala
ENST00000318024.8:c.1382A>C	ENSP00000317018.4:p.Glu461Ala
ENST00000526313.5:c.*96A>C	ENSP00000432236.1:n.*96A>C
ENST00000527020.5:c.1325A>C	ENSP00000436934.1:p.Glu442Ala
ENST00000527720.5:c.1289A>C	ENSP00000432944.1:p.Glu430Ala
ENST00000529563.5:n.266A>C
ENST00000534556.1:n.167A>C
NM_001297764.1:c.1325A>C	NP_001284693.1:p.Glu442Ala
NM_005709.3:c.1382A>C	NP_005700.2:p.Glu461Ala
NM_153676.3:c.2282A>C	NP_710142.1:p.Glu761Ala
NR_123738.1:n.1417A>C
XM_011519831.1:c.2306A>C	XP_011518133.1:p.Glu769Ala
XM_011519832.1:c.1535A>C	XP_011518134.1:p.Glu512Ala
XM_011519833.1:c.1432A>C	XP_011518135.1:p.Arg478=
XR_930841.1:n.1753A>C
XR_930842.1:n.1694A>C
XM_011519832.3:c.1535A>C	XP_011518134.1:p.Glu512Ala
XM_017017075.1:c.2282A>C	XP_016872564.1:p.Glu761Ala
XR_001747717.2:n.1541A>C
NM_153676.4:c.2282A>C MANE Select	NP_710142.1:p.Glu761Ala
NM_001297764.2:c.1325A>C	NP_001284693.1:p.Glu442Ala
NM_005709.4:c.1382A>C MANE Plus Clinical	NP_005700.2:p.Glu461Ala
NR_123738.2:n.1417A>C