Canonical Allele Identifier: CA2574769040

Gene: USH1C

Genomic Alleles

HGVS	Genome Assembly
NC_000011.10:g.17498292T>A , CM000673.2:g.17498292T>A	GRCh38
NC_000011.9:g.17519839T>A , CM000673.1:g.17519839T>A	GRCh37
NC_000011.8:g.17476415T>A	NCBI36
NG_011883.1:g.51125A>T
NG_011883.2:g.51125A>T

Transcript Alleles

HGVS	Amino-acid Change
ENST00000005226.12:c.2381-21A>T MANE Select	ENSP00000005226.7:n.2381-21A>T
ENST00000318024.9:c.1481-21A>T MANE Plus Clinical	ENSP00000317018.4:n.1481-21A>T
ENST00000005226.11:c.2381-21A>T	ENSP00000005226.7:n.2381-21A>T
ENST00000318024.8:c.1481-21A>T	ENSP00000317018.4:n.1481-21A>T
ENST00000526313.5:c.*195-21A>T	ENSP00000432236.1:n.*195-21A>T
ENST00000527020.5:c.1424-21A>T	ENSP00000436934.1:n.1424-21A>T
ENST00000527720.5:c.1388-21A>T	ENSP00000432944.1:n.1388-21A>T
ENST00000529563.5:n.365-21A>T
NM_001297764.1:c.1424-21A>T	NP_001284693.1:n.1424-21A>T
NM_005709.3:c.1481-21A>T	NP_005700.2:n.1481-21A>T
NM_153676.3:c.2381-21A>T	NP_710142.1:n.2381-21A>T
NR_123738.1:n.1516-21A>T
XM_011519831.1:c.2405-21A>T	XP_011518133.1:n.2405-21A>T
XM_011519832.1:c.1634-21A>T	XP_011518134.1:n.1634-21A>T
XM_011519832.3:c.1634-21A>T	XP_011518134.1:n.1634-21A>T
XM_017017075.1:c.2381-21A>T	XP_016872564.1:n.2381-21A>T
XR_001747717.2:n.1640-21A>T
NM_153676.4:c.2381-21A>T MANE Select	NP_710142.1:n.2381-21A>T
NM_001297764.2:c.1424-21A>T	NP_001284693.1:n.1424-21A>T
NM_005709.4:c.1481-21A>T MANE Plus Clinical	NP_005700.2:n.1481-21A>T
NR_123738.2:n.1516-21A>T