Canonical Allele Identifier: CA218486080

Gene: USH1C

Linked Data

• dbSNP Id: rs1053827086
• gnomAD v4: 11-17500953-G-A
• MyVariant Identifiers: chr11:g.17522500G>A (hg19) ; chr11:g.17500953G>A (hg38)

Genomic Alleles

HGVS	Genome Assembly
NC_000011.10:g.17500953G>A , CM000673.2:g.17500953G>A	GRCh38
NC_000011.9:g.17522500G>A , CM000673.1:g.17522500G>A	GRCh37
NC_000011.8:g.17479076G>A	NCBI36
NG_011883.1:g.48464C>T
NG_011883.2:g.48464C>T

Transcript Alleles

HGVS	Amino-acid change
ENST00000005226.12:c.2380+98C>T MANE Select	ENSP00000005226.7:n.2380+98C>T
ENST00000318024.9:c.1480+98C>T MANE Plus Clinical	ENSP00000317018.4:n.1480+98C>T
ENST00000005226.11:c.2380+98C>T	ENSP00000005226.7:n.2380+98C>T
ENST00000318024.8:c.1480+98C>T	ENSP00000317018.4:n.1480+98C>T
ENST00000526313.5:c.*194+98C>T	ENSP00000432236.1:n.*194+98C>T
ENST00000527020.5:c.1423+98C>T	ENSP00000436934.1:n.1423+98C>T
ENST00000527720.5:c.1387+98C>T	ENSP00000432944.1:n.1387+98C>T
ENST00000529563.5:n.364+98C>T
NM_001297764.1:c.1423+98C>T	NP_001284693.1:n.1423+98C>T
NM_005709.3:c.1480+98C>T	NP_005700.2:n.1480+98C>T
NM_153676.3:c.2380+98C>T	NP_710142.1:n.2380+98C>T
NR_123738.1:n.1515+98C>T
XM_011519831.1:c.2404+98C>T	XP_011518133.1:n.2404+98C>T
XM_011519832.1:c.1633+98C>T	XP_011518134.1:n.1633+98C>T
XM_011519832.3:c.1633+98C>T	XP_011518134.1:n.1633+98C>T
XM_017017075.1:c.2380+98C>T	XP_016872564.1:n.2380+98C>T
XR_001747717.2:n.1639+98C>T
NM_153676.4:c.2380+98C>T MANE Select	NP_710142.1:n.2380+98C>T
NM_001297764.2:c.1423+98C>T	NP_001284693.1:n.1423+98C>T
NM_005709.4:c.1480+98C>T MANE Plus Clinical	NP_005700.2:n.1480+98C>T
NR_123738.2:n.1515+98C>T