Canonical Allele Identifier: CA379800893

Gene: USH1C

Linked Data

• MyVariant Identifiers: chr11:g.17519760G>T (hg19) ; chr11:g.17498213G>T (hg38)

Genomic Alleles

HGVS	Genome Assembly
NC_000011.10:g.17498213G>T , CM000673.2:g.17498213G>T	GRCh38
NC_000011.9:g.17519760G>T , CM000673.1:g.17519760G>T	GRCh37
NC_000011.8:g.17476336G>T	NCBI36
NG_011883.1:g.51204C>A
NG_011883.2:g.51204C>A

Transcript Alleles

HGVS	Amino-acid change
ENST00000005226.12:c.2439C>A MANE Select	ENSP00000005226.7:p.Tyr813Ter
ENST00000318024.9:c.1539C>A MANE Plus Clinical	ENSP00000317018.4:p.Tyr513Ter
ENST00000005226.11:c.2439C>A	ENSP00000005226.7:p.Tyr813Ter
ENST00000318024.8:c.1539C>A	ENSP00000317018.4:p.Tyr513Ter
ENST00000526313.5:c.*253C>A	ENSP00000432236.1:n.*253C>A
ENST00000527020.5:c.1482C>A	ENSP00000436934.1:p.Tyr494Ter
ENST00000527720.5:c.1446C>A	ENSP00000432944.1:p.Tyr482Ter
ENST00000529563.5:n.423C>A
NM_001297764.1:c.1482C>A	NP_001284693.1:p.Tyr494Ter
NM_005709.3:c.1539C>A	NP_005700.2:p.Tyr513Ter
NM_153676.3:c.2439C>A	NP_710142.1:p.Tyr813Ter
NR_123738.1:n.1574C>A
XM_011519831.1:c.2463C>A	XP_011518133.1:p.Tyr821Ter
XM_011519832.1:c.1692C>A	XP_011518134.1:p.Tyr564Ter
XM_011519832.3:c.1692C>A	XP_011518134.1:p.Tyr564Ter
XM_017017075.1:c.2439C>A	XP_016872564.1:p.Tyr813Ter
XR_001747717.2:n.1698C>A
NM_153676.4:c.2439C>A MANE Select	NP_710142.1:p.Tyr813Ter
NM_001297764.2:c.1482C>A	NP_001284693.1:p.Tyr494Ter
NM_005709.4:c.1539C>A MANE Plus Clinical	NP_005700.2:p.Tyr513Ter
NR_123738.2:n.1574C>A