Canonical Allele Identifier: CA379803382

Gene: USH1C

Linked Data

• MyVariant Identifiers: chr11:g.17523042A>T (hg19) ; chr11:g.17501495A>T (hg38)

Genomic Alleles

HGVS	Genome Assembly
NC_000011.10:g.17501495A>T , CM000673.2:g.17501495A>T	GRCh38
NC_000011.9:g.17523042A>T , CM000673.1:g.17523042A>T	GRCh37
NC_000011.8:g.17479618A>T	NCBI36
NG_011883.1:g.47922T>A
NG_011883.2:g.47922T>A

Transcript Alleles

HGVS	Amino-acid Change
ENST00000005226.12:c.2267T>A MANE Select	ENSP00000005226.7:p.Leu756Gln
ENST00000318024.9:c.1367T>A MANE Plus Clinical	ENSP00000317018.4:p.Leu456Gln
ENST00000005226.11:c.2267T>A	ENSP00000005226.7:p.Leu756Gln
ENST00000318024.8:c.1367T>A	ENSP00000317018.4:p.Leu456Gln
ENST00000526313.5:c.*81T>A	ENSP00000432236.1:n.*81T>A
ENST00000527020.5:c.1310T>A	ENSP00000436934.1:p.Leu437Gln
ENST00000527720.5:c.1274T>A	ENSP00000432944.1:p.Leu425Gln
ENST00000529563.5:n.251T>A
ENST00000534556.1:n.152T>A
NM_001297764.1:c.1310T>A	NP_001284693.1:p.Leu437Gln
NM_005709.3:c.1367T>A	NP_005700.2:p.Leu456Gln
NM_153676.3:c.2267T>A	NP_710142.1:p.Leu756Gln
NR_123738.1:n.1402T>A
XM_011519831.1:c.2291T>A	XP_011518133.1:p.Leu764Gln
XM_011519832.1:c.1520T>A	XP_011518134.1:p.Leu507Gln
XM_011519833.1:c.1417T>A	XP_011518135.1:p.Tyr473Asn
XR_930841.1:n.1738T>A
XR_930842.1:n.1679T>A
XM_011519832.3:c.1520T>A	XP_011518134.1:p.Leu507Gln
XM_017017075.1:c.2267T>A	XP_016872564.1:p.Leu756Gln
XR_001747717.2:n.1526T>A
NM_153676.4:c.2267T>A MANE Select	NP_710142.1:p.Leu756Gln
NM_001297764.2:c.1310T>A	NP_001284693.1:p.Leu437Gln
NM_005709.4:c.1367T>A MANE Plus Clinical	NP_005700.2:p.Leu456Gln
NR_123738.2:n.1402T>A