Canonical Allele Identifier: CA379800995

Gene: USH1C

Linked Data

• MyVariant Identifiers: chr11:g.17519770A>C (hg19) ; chr11:g.17498223A>C (hg38)

Genomic Alleles

HGVS	Genome Assembly
NC_000011.10:g.17498223A>C , CM000673.2:g.17498223A>C	GRCh38
NC_000011.9:g.17519770A>C , CM000673.1:g.17519770A>C	GRCh37
NC_000011.8:g.17476346A>C	NCBI36
NG_011883.1:g.51194T>G
NG_011883.2:g.51194T>G

Transcript Alleles

HGVS	Amino-acid Change
ENST00000005226.12:c.2429T>G MANE Select	ENSP00000005226.7:p.Val810Gly
ENST00000318024.9:c.1529T>G MANE Plus Clinical	ENSP00000317018.4:p.Val510Gly
ENST00000005226.11:c.2429T>G	ENSP00000005226.7:p.Val810Gly
ENST00000318024.8:c.1529T>G	ENSP00000317018.4:p.Val510Gly
ENST00000526313.5:c.*243T>G	ENSP00000432236.1:n.*243T>G
ENST00000527020.5:c.1472T>G	ENSP00000436934.1:p.Val491Gly
ENST00000527720.5:c.1436T>G	ENSP00000432944.1:p.Val479Gly
ENST00000529563.5:n.413T>G
NM_001297764.1:c.1472T>G	NP_001284693.1:p.Val491Gly
NM_005709.3:c.1529T>G	NP_005700.2:p.Val510Gly
NM_153676.3:c.2429T>G	NP_710142.1:p.Val810Gly
NR_123738.1:n.1564T>G
XM_011519831.1:c.2453T>G	XP_011518133.1:p.Val818Gly
XM_011519832.1:c.1682T>G	XP_011518134.1:p.Val561Gly
XM_011519832.3:c.1682T>G	XP_011518134.1:p.Val561Gly
XM_017017075.1:c.2429T>G	XP_016872564.1:p.Val810Gly
XR_001747717.2:n.1688T>G
NM_153676.4:c.2429T>G MANE Select	NP_710142.1:p.Val810Gly
NM_001297764.2:c.1472T>G	NP_001284693.1:p.Val491Gly
NM_005709.4:c.1529T>G MANE Plus Clinical	NP_005700.2:p.Val510Gly
NR_123738.2:n.1564T>G