Canonical Allele Identifier: CA379800762

Gene: USH1C

Linked Data

• MyVariant Identifiers: chr11:g.17519748C>A (hg19) ; chr11:g.17498201C>A (hg38)

Genomic Alleles

HGVS	Genome Assembly
NC_000011.10:g.17498201C>A , CM000673.2:g.17498201C>A	GRCh38
NC_000011.9:g.17519748C>A , CM000673.1:g.17519748C>A	GRCh37
NC_000011.8:g.17476324C>A	NCBI36
NG_011883.1:g.51216G>T
NG_011883.2:g.51216G>T

Transcript Alleles

HGVS	Amino-acid change
ENST00000005226.12:c.2451G>T MANE Select	ENSP00000005226.7:p.Glu817Asp
ENST00000318024.9:c.1551G>T MANE Plus Clinical	ENSP00000317018.4:p.Glu517Asp
ENST00000005226.11:c.2451G>T	ENSP00000005226.7:p.Glu817Asp
ENST00000318024.8:c.1551G>T	ENSP00000317018.4:p.Glu517Asp
ENST00000526313.5:c.*265G>T	ENSP00000432236.1:n.*265G>T
ENST00000527020.5:c.1494G>T	ENSP00000436934.1:p.Glu498Asp
ENST00000527720.5:c.1458G>T	ENSP00000432944.1:p.Glu486Asp
ENST00000529563.5:n.435G>T
NM_001297764.1:c.1494G>T	NP_001284693.1:p.Glu498Asp
NM_005709.3:c.1551G>T	NP_005700.2:p.Glu517Asp
NM_153676.3:c.2451G>T	NP_710142.1:p.Glu817Asp
NR_123738.1:n.1586G>T
XM_011519831.1:c.2475G>T	XP_011518133.1:p.Glu825Asp
XM_011519832.1:c.1704G>T	XP_011518134.1:p.Glu568Asp
XM_011519832.3:c.1704G>T	XP_011518134.1:p.Glu568Asp
XM_017017075.1:c.2451G>T	XP_016872564.1:p.Glu817Asp
XR_001747717.2:n.1710G>T
NM_153676.4:c.2451G>T MANE Select	NP_710142.1:p.Glu817Asp
NM_001297764.2:c.1494G>T	NP_001284693.1:p.Glu498Asp
NM_005709.4:c.1551G>T MANE Plus Clinical	NP_005700.2:p.Glu517Asp
NR_123738.2:n.1586G>T