Canonical Allele Identifier: CA473304946

Gene: USH1C

Linked Data

• MyVariant Identifiers: chr11:g.17519751A>C (hg19)

Genomic Alleles

HGVS	Genome Assembly
NC_000011.10:g.17498204A>C , CM000673.2:g.17498204A>C	GRCh38
NC_000011.9:g.17519751A>C , CM000673.1:g.17519751A>C	GRCh37
NC_000011.8:g.17476327A>C	NCBI36
NG_011883.1:g.51213T>G
NG_011883.2:g.51213T>G

Transcript Alleles

HGVS	Amino-acid change
ENST00000005226.12:c.2448T>G MANE Select	ENSP00000005226.7:p.Ala816=
ENST00000318024.9:c.1548T>G MANE Plus Clinical	ENSP00000317018.4:p.Ala516=
ENST00000005226.11:c.2448T>G	ENSP00000005226.7:p.Ala816=
ENST00000318024.8:c.1548T>G	ENSP00000317018.4:p.Ala516=
ENST00000526313.5:c.*262T>G	ENSP00000432236.1:n.*262T>G
ENST00000527020.5:c.1491T>G	ENSP00000436934.1:p.Ala497=
ENST00000527720.5:c.1455T>G	ENSP00000432944.1:p.Ala485=
ENST00000529563.5:n.432T>G
NM_001297764.1:c.1491T>G	NP_001284693.1:p.Ala497=
NM_005709.3:c.1548T>G	NP_005700.2:p.Ala516=
NM_153676.3:c.2448T>G	NP_710142.1:p.Ala816=
NR_123738.1:n.1583T>G
XM_011519831.1:c.2472T>G	XP_011518133.1:p.Ala824=
XM_011519832.1:c.1701T>G	XP_011518134.1:p.Ala567=
XM_011519832.3:c.1701T>G	XP_011518134.1:p.Ala567=
XM_017017075.1:c.2448T>G	XP_016872564.1:p.Ala816=
XR_001747717.2:n.1707T>G
NM_153676.4:c.2448T>G MANE Select	NP_710142.1:p.Ala816=
NM_001297764.2:c.1491T>G	NP_001284693.1:p.Ala497=
NM_005709.4:c.1548T>G MANE Plus Clinical	NP_005700.2:p.Ala516=
NR_123738.2:n.1583T>G