Canonical Allele Identifier: CA379803144

Gene: USH1C

Linked Data

• MyVariant Identifiers: chr11:g.17522671T>A (hg19) ; chr11:g.17501124T>A (hg38)

Genomic Alleles

HGVS	Genome Assembly
NC_000011.10:g.17501124T>A , CM000673.2:g.17501124T>A	GRCh38
NC_000011.9:g.17522671T>A , CM000673.1:g.17522671T>A	GRCh37
NC_000011.8:g.17479247T>A	NCBI36
NG_011883.1:g.48293A>T
NG_011883.2:g.48293A>T

Transcript Alleles

HGVS	Amino-acid Change
ENST00000005226.12:c.2307A>T MANE Select	ENSP00000005226.7:p.Glu769Asp
ENST00000318024.9:c.1407A>T MANE Plus Clinical	ENSP00000317018.4:p.Glu469Asp
ENST00000005226.11:c.2307A>T	ENSP00000005226.7:p.Glu769Asp
ENST00000318024.8:c.1407A>T	ENSP00000317018.4:p.Glu469Asp
ENST00000526313.5:c.*121A>T	ENSP00000432236.1:n.*121A>T
ENST00000527020.5:c.1350A>T	ENSP00000436934.1:p.Glu450Asp
ENST00000527720.5:c.1314A>T	ENSP00000432944.1:p.Glu438Asp
ENST00000529563.5:n.291A>T
ENST00000534556.1:n.192A>T
NM_001297764.1:c.1350A>T	NP_001284693.1:p.Glu450Asp
NM_005709.3:c.1407A>T	NP_005700.2:p.Glu469Asp
NM_153676.3:c.2307A>T	NP_710142.1:p.Glu769Asp
NR_123738.1:n.1442A>T
XM_011519831.1:c.2331A>T	XP_011518133.1:p.Glu777Asp
XM_011519832.1:c.1560A>T	XP_011518134.1:p.Glu520Asp
XM_011519833.1:c.*14A>T	XP_011518135.1:n.*14A>T
XR_930841.1:n.1778A>T
XR_930842.1:n.1719A>T
XM_011519832.3:c.1560A>T	XP_011518134.1:p.Glu520Asp
XM_017017075.1:c.2307A>T	XP_016872564.1:p.Glu769Asp
XR_001747717.2:n.1566A>T
NM_153676.4:c.2307A>T MANE Select	NP_710142.1:p.Glu769Asp
NM_001297764.2:c.1350A>T	NP_001284693.1:p.Glu450Asp
NM_005709.4:c.1407A>T MANE Plus Clinical	NP_005700.2:p.Glu469Asp
NR_123738.2:n.1442A>T