Canonical Allele Identifier: CA379803443

Gene: USH1C

Linked Data

• MyVariant Identifiers: chr11:g.17523051A>T (hg19) ; chr11:g.17501504A>T (hg38)

Genomic Alleles

HGVS	Genome Assembly
NC_000011.10:g.17501504A>T , CM000673.2:g.17501504A>T	GRCh38
NC_000011.9:g.17523051A>T , CM000673.1:g.17523051A>T	GRCh37
NC_000011.8:g.17479627A>T	NCBI36
NG_011883.1:g.47913T>A
NG_011883.2:g.47913T>A

Transcript Alleles

HGVS	Amino-acid Change
ENST00000005226.12:c.2258T>A MANE Select	ENSP00000005226.7:p.Val753Asp
ENST00000318024.9:c.1358T>A MANE Plus Clinical	ENSP00000317018.4:p.Val453Asp
ENST00000005226.11:c.2258T>A	ENSP00000005226.7:p.Val753Asp
ENST00000318024.8:c.1358T>A	ENSP00000317018.4:p.Val453Asp
ENST00000526313.5:c.*72T>A	ENSP00000432236.1:n.*72T>A
ENST00000527020.5:c.1301T>A	ENSP00000436934.1:p.Val434Asp
ENST00000527720.5:c.1265T>A	ENSP00000432944.1:p.Val422Asp
ENST00000529563.5:n.242T>A
ENST00000534556.1:n.143T>A
NM_001297764.1:c.1301T>A	NP_001284693.1:p.Val434Asp
NM_005709.3:c.1358T>A	NP_005700.2:p.Val453Asp
NM_153676.3:c.2258T>A	NP_710142.1:p.Val753Asp
NR_123738.1:n.1393T>A
XM_011519831.1:c.2282T>A	XP_011518133.1:p.Val761Asp
XM_011519832.1:c.1511T>A	XP_011518134.1:p.Val504Asp
XM_011519833.1:c.1408T>A	XP_011518135.1:p.Ser470Thr
XR_930841.1:n.1729T>A
XR_930842.1:n.1670T>A
XM_011519832.3:c.1511T>A	XP_011518134.1:p.Val504Asp
XM_017017075.1:c.2258T>A	XP_016872564.1:p.Val753Asp
XR_001747717.2:n.1517T>A
NM_153676.4:c.2258T>A MANE Select	NP_710142.1:p.Val753Asp
NM_001297764.2:c.1301T>A	NP_001284693.1:p.Val434Asp
NM_005709.4:c.1358T>A MANE Plus Clinical	NP_005700.2:p.Val453Asp
NR_123738.2:n.1393T>A