Canonical Allele Identifier: CA379802921

Gene: USH1C

Linked Data

• MyVariant Identifiers: chr11:g.17522610C>A (hg19) ; chr11:g.17501063C>A (hg38)

Genomic Alleles

HGVS	Genome Assembly
NC_000011.10:g.17501063C>A , CM000673.2:g.17501063C>A	GRCh38
NC_000011.9:g.17522610C>A , CM000673.1:g.17522610C>A	GRCh37
NC_000011.8:g.17479186C>A	NCBI36
NG_011883.1:g.48354G>T
NG_011883.2:g.48354G>T

Transcript Alleles

HGVS	Amino-acid change
ENST00000005226.12:c.2368G>T MANE Select	ENSP00000005226.7:p.Ala790Ser
ENST00000318024.9:c.1468G>T MANE Plus Clinical	ENSP00000317018.4:p.Ala490Ser
ENST00000005226.11:c.2368G>T	ENSP00000005226.7:p.Ala790Ser
ENST00000318024.8:c.1468G>T	ENSP00000317018.4:p.Ala490Ser
ENST00000526313.5:c.*182G>T	ENSP00000432236.1:n.*182G>T
ENST00000527020.5:c.1411G>T	ENSP00000436934.1:p.Ala471Ser
ENST00000527720.5:c.1375G>T	ENSP00000432944.1:p.Ala459Ser
ENST00000529563.5:n.352G>T
NM_001297764.1:c.1411G>T	NP_001284693.1:p.Ala471Ser
NM_005709.3:c.1468G>T	NP_005700.2:p.Ala490Ser
NM_153676.3:c.2368G>T	NP_710142.1:p.Ala790Ser
NR_123738.1:n.1503G>T
XM_011519831.1:c.2392G>T	XP_011518133.1:p.Ala798Ser
XM_011519832.1:c.1621G>T	XP_011518134.1:p.Ala541Ser
XM_011519833.1:c.*75G>T	XP_011518135.1:n.*75G>T
XR_930841.1:n.1839G>T
XR_930842.1:n.1780G>T
XM_011519832.3:c.1621G>T	XP_011518134.1:p.Ala541Ser
XM_017017075.1:c.2368G>T	XP_016872564.1:p.Ala790Ser
XR_001747717.2:n.1627G>T
NM_153676.4:c.2368G>T MANE Select	NP_710142.1:p.Ala790Ser
NM_001297764.2:c.1411G>T	NP_001284693.1:p.Ala471Ser
NM_005709.4:c.1468G>T MANE Plus Clinical	NP_005700.2:p.Ala490Ser
NR_123738.2:n.1503G>T