Canonical Allele Identifier: CA379803430

Gene: USH1C

Linked Data

• MyVariant Identifiers: chr11:g.17523049G>C (hg19) ; chr11:g.17501502G>C (hg38)

Genomic Alleles

HGVS	Genome Assembly
NC_000011.10:g.17501502G>C , CM000673.2:g.17501502G>C	GRCh38
NC_000011.9:g.17523049G>C , CM000673.1:g.17523049G>C	GRCh37
NC_000011.8:g.17479625G>C	NCBI36
NG_011883.1:g.47915C>G
NG_011883.2:g.47915C>G

Transcript Alleles

HGVS	Amino-acid Change
ENST00000005226.12:c.2260C>G MANE Select	ENSP00000005226.7:p.Arg754Gly
ENST00000318024.9:c.1360C>G MANE Plus Clinical	ENSP00000317018.4:p.Arg454Gly
ENST00000005226.11:c.2260C>G	ENSP00000005226.7:p.Arg754Gly
ENST00000318024.8:c.1360C>G	ENSP00000317018.4:p.Arg454Gly
ENST00000526313.5:c.*74C>G	ENSP00000432236.1:n.*74C>G
ENST00000527020.5:c.1303C>G	ENSP00000436934.1:p.Arg435Gly
ENST00000527720.5:c.1267C>G	ENSP00000432944.1:p.Arg423Gly
ENST00000529563.5:n.244C>G
ENST00000534556.1:n.145C>G
NM_001297764.1:c.1303C>G	NP_001284693.1:p.Arg435Gly
NM_005709.3:c.1360C>G	NP_005700.2:p.Arg454Gly
NM_153676.3:c.2260C>G	NP_710142.1:p.Arg754Gly
NR_123738.1:n.1395C>G
XM_011519831.1:c.2284C>G	XP_011518133.1:p.Arg762Gly
XM_011519832.1:c.1513C>G	XP_011518134.1:p.Arg505Gly
XM_011519833.1:c.1410C>G	XP_011518135.1:p.Ser470=
XR_930841.1:n.1731C>G
XR_930842.1:n.1672C>G
XM_011519832.3:c.1513C>G	XP_011518134.1:p.Arg505Gly
XM_017017075.1:c.2260C>G	XP_016872564.1:p.Arg754Gly
XR_001747717.2:n.1519C>G
NM_153676.4:c.2260C>G MANE Select	NP_710142.1:p.Arg754Gly
NM_001297764.2:c.1303C>G	NP_001284693.1:p.Arg435Gly
NM_005709.4:c.1360C>G MANE Plus Clinical	NP_005700.2:p.Arg454Gly
NR_123738.2:n.1395C>G