Canonical Allele Identifier: CA379795168

Gene: USH1C

Linked Data

• gnomAD v4: 11-17527235-T-C
• MyVariant Identifiers: chr11:g.17548782T>C (hg19) ; chr11:g.17527235T>C (hg38)

Genomic Alleles

HGVS	Genome Assembly
NC_000011.10:g.17527235T>C , CM000673.2:g.17527235T>C	GRCh38
NC_000011.9:g.17548782T>C , CM000673.1:g.17548782T>C	GRCh37
NC_000011.8:g.17505358T>C	NCBI36
NG_011883.1:g.22182A>G
NG_011883.2:g.22182A>G

Transcript Alleles

HGVS	Amino-acid Change
ENST00000005226.12:c.484A>G MANE Select	ENSP00000005226.7:p.Ile162Val
ENST00000318024.9:c.484A>G MANE Plus Clinical	ENSP00000317018.4:p.Ile162Val
ENST00000005226.11:c.484A>G	ENSP00000005226.7:p.Ile162Val
ENST00000318024.8:c.484A>G	ENSP00000317018.4:p.Ile162Val
ENST00000526181.1:c.517A>G	ENSP00000437128.1:p.Ile173Val
ENST00000526313.5:c.484A>G	ENSP00000432236.1:p.Ile162Val
ENST00000527020.5:c.484A>G	ENSP00000436934.1:p.Ile162Val
ENST00000527720.5:c.391A>G	ENSP00000432944.1:p.Ile131Val
NM_001297764.1:c.484A>G	NP_001284693.1:p.Ile162Val
NM_005709.3:c.484A>G	NP_005700.2:p.Ile162Val
NM_153676.3:c.484A>G	NP_710142.1:p.Ile162Val
NR_123738.1:n.593A>G
XM_011519831.1:c.484A>G	XP_011518133.1:p.Ile162Val
XM_011519832.1:c.484A>G	XP_011518134.1:p.Ile162Val
XM_011519833.1:c.484A>G	XP_011518135.1:p.Ile162Val
XM_011519834.1:c.484A>G	XP_011518136.1:p.Ile162Val
XR_930841.1:n.593A>G
XR_930842.1:n.593A>G
XM_011519832.3:c.484A>G	XP_011518134.1:p.Ile162Val
XM_011519834.2:c.484A>G	XP_011518136.1:p.Ile162Val
XM_017017072.1:c.484A>G	XP_016872561.1:p.Ile162Val
XM_017017073.1:c.484A>G	XP_016872562.1:p.Ile162Val
XM_017017074.1:c.484A>G	XP_016872563.1:p.Ile162Val
XM_017017075.1:c.484A>G	XP_016872564.1:p.Ile162Val
XR_001747717.2:n.593A>G
NM_153676.4:c.484A>G MANE Select	NP_710142.1:p.Ile162Val
NM_001297764.2:c.484A>G	NP_001284693.1:p.Ile162Val
NM_005709.4:c.484A>G MANE Plus Clinical	NP_005700.2:p.Ile162Val
NR_123738.2:n.593A>G