Canonical Allele Identifier: CA379801037

Gene: USH1C

Linked Data

• MyVariant Identifiers: chr11:g.17519774T>C (hg19) ; chr11:g.17498227T>C (hg38)

Genomic Alleles

HGVS	Genome Assembly
NC_000011.10:g.17498227T>C , CM000673.2:g.17498227T>C	GRCh38
NC_000011.9:g.17519774T>C , CM000673.1:g.17519774T>C	GRCh37
NC_000011.8:g.17476350T>C	NCBI36
NG_011883.1:g.51190A>G
NG_011883.2:g.51190A>G

Transcript Alleles

HGVS	Amino-acid Change
ENST00000005226.12:c.2425A>G MANE Select	ENSP00000005226.7:p.Ile809Val
ENST00000318024.9:c.1525A>G MANE Plus Clinical	ENSP00000317018.4:p.Ile509Val
ENST00000005226.11:c.2425A>G	ENSP00000005226.7:p.Ile809Val
ENST00000318024.8:c.1525A>G	ENSP00000317018.4:p.Ile509Val
ENST00000526313.5:c.*239A>G	ENSP00000432236.1:n.*239A>G
ENST00000527020.5:c.1468A>G	ENSP00000436934.1:p.Ile490Val
ENST00000527720.5:c.1432A>G	ENSP00000432944.1:p.Ile478Val
ENST00000529563.5:n.409A>G
NM_001297764.1:c.1468A>G	NP_001284693.1:p.Ile490Val
NM_005709.3:c.1525A>G	NP_005700.2:p.Ile509Val
NM_153676.3:c.2425A>G	NP_710142.1:p.Ile809Val
NR_123738.1:n.1560A>G
XM_011519831.1:c.2449A>G	XP_011518133.1:p.Ile817Val
XM_011519832.1:c.1678A>G	XP_011518134.1:p.Ile560Val
XM_011519832.3:c.1678A>G	XP_011518134.1:p.Ile560Val
XM_017017075.1:c.2425A>G	XP_016872564.1:p.Ile809Val
XR_001747717.2:n.1684A>G
NM_153676.4:c.2425A>G MANE Select	NP_710142.1:p.Ile809Val
NM_001297764.2:c.1468A>G	NP_001284693.1:p.Ile490Val
NM_005709.4:c.1525A>G MANE Plus Clinical	NP_005700.2:p.Ile509Val
NR_123738.2:n.1560A>G