Canonical Allele Identifier: CA473305290

Gene: USH1C

Linked Data

• MyVariant Identifiers: chr11:g.17522638G>C (hg19)

Genomic Alleles

HGVS	Genome Assembly
NC_000011.10:g.17501091G>C , CM000673.2:g.17501091G>C	GRCh38
NC_000011.9:g.17522638G>C , CM000673.1:g.17522638G>C	GRCh37
NC_000011.8:g.17479214G>C	NCBI36
NG_011883.1:g.48326C>G
NG_011883.2:g.48326C>G

Transcript Alleles

HGVS	Amino-acid Change
ENST00000005226.12:c.2340C>G MANE Select	ENSP00000005226.7:p.Val780=
ENST00000318024.9:c.1440C>G MANE Plus Clinical	ENSP00000317018.4:p.Val480=
ENST00000005226.11:c.2340C>G	ENSP00000005226.7:p.Val780=
ENST00000318024.8:c.1440C>G	ENSP00000317018.4:p.Val480=
ENST00000526313.5:c.*154C>G	ENSP00000432236.1:n.*154C>G
ENST00000527020.5:c.1383C>G	ENSP00000436934.1:p.Val461=
ENST00000527720.5:c.1347C>G	ENSP00000432944.1:p.Val449=
ENST00000529563.5:n.324C>G
ENST00000534556.1:n.225C>G
NM_001297764.1:c.1383C>G	NP_001284693.1:p.Val461=
NM_005709.3:c.1440C>G	NP_005700.2:p.Val480=
NM_153676.3:c.2340C>G	NP_710142.1:p.Val780=
NR_123738.1:n.1475C>G
XM_011519831.1:c.2364C>G	XP_011518133.1:p.Val788=
XM_011519832.1:c.1593C>G	XP_011518134.1:p.Val531=
XM_011519833.1:c.*47C>G	XP_011518135.1:n.*47C>G
XR_930841.1:n.1811C>G
XR_930842.1:n.1752C>G
XM_011519832.3:c.1593C>G	XP_011518134.1:p.Val531=
XM_017017075.1:c.2340C>G	XP_016872564.1:p.Val780=
XR_001747717.2:n.1599C>G
NM_153676.4:c.2340C>G MANE Select	NP_710142.1:p.Val780=
NM_001297764.2:c.1383C>G	NP_001284693.1:p.Val461=
NM_005709.4:c.1440C>G MANE Plus Clinical	NP_005700.2:p.Val480=
NR_123738.2:n.1475C>G