Canonical Allele Identifier: CA379803328

Gene: USH1C

Linked Data

• dbSNP Id: rs1432013715
• gnomAD v2: 11-17523033-T-C
• gnomAD v4: 11-17501486-T-C
• MyVariant Identifiers: chr11:g.17523033T>C (hg19) ; chr11:g.17501486T>C (hg38)

Genomic Alleles

HGVS	Genome Assembly
NC_000011.10:g.17501486T>C , CM000673.2:g.17501486T>C	GRCh38
NC_000011.9:g.17523033T>C , CM000673.1:g.17523033T>C	GRCh37
NC_000011.8:g.17479609T>C	NCBI36
NG_011883.1:g.47931A>G
NG_011883.2:g.47931A>G

Transcript Alleles

HGVS	Amino-acid Change
ENST00000005226.12:c.2276A>G MANE Select	ENSP00000005226.7:p.Lys759Arg
ENST00000318024.9:c.1376A>G MANE Plus Clinical	ENSP00000317018.4:p.Lys459Arg
ENST00000005226.11:c.2276A>G	ENSP00000005226.7:p.Lys759Arg
ENST00000318024.8:c.1376A>G	ENSP00000317018.4:p.Lys459Arg
ENST00000526313.5:c.*90A>G	ENSP00000432236.1:n.*90A>G
ENST00000527020.5:c.1319A>G	ENSP00000436934.1:p.Lys440Arg
ENST00000527720.5:c.1283A>G	ENSP00000432944.1:p.Lys428Arg
ENST00000529563.5:n.260A>G
ENST00000534556.1:n.161A>G
NM_001297764.1:c.1319A>G	NP_001284693.1:p.Lys440Arg
NM_005709.3:c.1376A>G	NP_005700.2:p.Lys459Arg
NM_153676.3:c.2276A>G	NP_710142.1:p.Lys759Arg
NR_123738.1:n.1411A>G
XM_011519831.1:c.2300A>G	XP_011518133.1:p.Lys767Arg
XM_011519832.1:c.1529A>G	XP_011518134.1:p.Lys510Arg
XM_011519833.1:c.1426A>G	XP_011518135.1:p.Arg476Gly
XR_930841.1:n.1747A>G
XR_930842.1:n.1688A>G
XM_011519832.3:c.1529A>G	XP_011518134.1:p.Lys510Arg
XM_017017075.1:c.2276A>G	XP_016872564.1:p.Lys759Arg
XR_001747717.2:n.1535A>G
NM_153676.4:c.2276A>G MANE Select	NP_710142.1:p.Lys759Arg
NM_001297764.2:c.1319A>G	NP_001284693.1:p.Lys440Arg
NM_005709.4:c.1376A>G MANE Plus Clinical	NP_005700.2:p.Lys459Arg
NR_123738.2:n.1411A>G