Canonical Allele Identifier: CA473305293

Gene: USH1C

Linked Data

• MyVariant Identifiers: chr11:g.17522641C>T (hg19)

Genomic Alleles

HGVS	Genome Assembly
NC_000011.10:g.17501094C>T , CM000673.2:g.17501094C>T	GRCh38
NC_000011.9:g.17522641C>T , CM000673.1:g.17522641C>T	GRCh37
NC_000011.8:g.17479217C>T	NCBI36
NG_011883.1:g.48323G>A
NG_011883.2:g.48323G>A

Transcript Alleles

HGVS	Amino-acid Change
ENST00000005226.12:c.2337G>A MANE Select	ENSP00000005226.7:p.Val779=
ENST00000318024.9:c.1437G>A MANE Plus Clinical	ENSP00000317018.4:p.Val479=
ENST00000005226.11:c.2337G>A	ENSP00000005226.7:p.Val779=
ENST00000318024.8:c.1437G>A	ENSP00000317018.4:p.Val479=
ENST00000526313.5:c.*151G>A	ENSP00000432236.1:n.*151G>A
ENST00000527020.5:c.1380G>A	ENSP00000436934.1:p.Val460=
ENST00000527720.5:c.1344G>A	ENSP00000432944.1:p.Val448=
ENST00000529563.5:n.321G>A
ENST00000534556.1:n.222G>A
NM_001297764.1:c.1380G>A	NP_001284693.1:p.Val460=
NM_005709.3:c.1437G>A	NP_005700.2:p.Val479=
NM_153676.3:c.2337G>A	NP_710142.1:p.Val779=
NR_123738.1:n.1472G>A
XM_011519831.1:c.2361G>A	XP_011518133.1:p.Val787=
XM_011519832.1:c.1590G>A	XP_011518134.1:p.Val530=
XM_011519833.1:c.*44G>A	XP_011518135.1:n.*44G>A
XR_930841.1:n.1808G>A
XR_930842.1:n.1749G>A
XM_011519832.3:c.1590G>A	XP_011518134.1:p.Val530=
XM_017017075.1:c.2337G>A	XP_016872564.1:p.Val779=
XR_001747717.2:n.1596G>A
NM_153676.4:c.2337G>A MANE Select	NP_710142.1:p.Val779=
NM_001297764.2:c.1380G>A	NP_001284693.1:p.Val460=
NM_005709.4:c.1437G>A MANE Plus Clinical	NP_005700.2:p.Val479=
NR_123738.2:n.1472G>A