Canonical Allele Identifier: CA379801360

Gene: USH1C

Linked Data

• MyVariant Identifiers: chr11:g.17519809A>G (hg19) ; chr11:g.17498262A>G (hg38)

Genomic Alleles

HGVS	Genome Assembly
NC_000011.10:g.17498262A>G , CM000673.2:g.17498262A>G	GRCh38
NC_000011.9:g.17519809A>G , CM000673.1:g.17519809A>G	GRCh37
NC_000011.8:g.17476385A>G	NCBI36
NG_011883.1:g.51155T>C
NG_011883.2:g.51155T>C

Transcript Alleles

HGVS	Amino-acid Change
ENST00000005226.12:c.2390T>C MANE Select	ENSP00000005226.7:p.Val797Ala
ENST00000318024.9:c.1490T>C MANE Plus Clinical	ENSP00000317018.4:p.Val497Ala
ENST00000005226.11:c.2390T>C	ENSP00000005226.7:p.Val797Ala
ENST00000318024.8:c.1490T>C	ENSP00000317018.4:p.Val497Ala
ENST00000526313.5:c.*204T>C	ENSP00000432236.1:n.*204T>C
ENST00000527020.5:c.1433T>C	ENSP00000436934.1:p.Val478Ala
ENST00000527720.5:c.1397T>C	ENSP00000432944.1:p.Val466Ala
ENST00000529563.5:n.374T>C
NM_001297764.1:c.1433T>C	NP_001284693.1:p.Val478Ala
NM_005709.3:c.1490T>C	NP_005700.2:p.Val497Ala
NM_153676.3:c.2390T>C	NP_710142.1:p.Val797Ala
NR_123738.1:n.1525T>C
XM_011519831.1:c.2414T>C	XP_011518133.1:p.Val805Ala
XM_011519832.1:c.1643T>C	XP_011518134.1:p.Val548Ala
XM_011519832.3:c.1643T>C	XP_011518134.1:p.Val548Ala
XM_017017075.1:c.2390T>C	XP_016872564.1:p.Val797Ala
XR_001747717.2:n.1649T>C
NM_153676.4:c.2390T>C MANE Select	NP_710142.1:p.Val797Ala
NM_001297764.2:c.1433T>C	NP_001284693.1:p.Val478Ala
NM_005709.4:c.1490T>C MANE Plus Clinical	NP_005700.2:p.Val497Ala
NR_123738.2:n.1525T>C