Canonical Allele Identifier: CA1955173145

Gene: USH1C

Linked Data

• dbSNP Id: rs1849414901
• gnomAD v4: 11-17500971-GTCA-G

Genomic Alleles

HGVS	Genome Assembly
NC_000011.10:g.17500972_17500974del , CM000673.2:g.17500972_17500974del	GRCh38
NC_000011.9:g.17522519_17522521del , CM000673.1:g.17522519_17522521del	GRCh37
NC_000011.8:g.17479095_17479097del	NCBI36
NG_011883.1:g.48443_48445del
NG_011883.2:g.48443_48445del

Transcript Alleles

HGVS	Amino-acid change
ENST00000005226.12:c.2380+77_2380+79del MANE Select	ENSP00000005226.7:n.2380+77_2380+79del
ENST00000318024.9:c.1480+77_1480+79del MANE Plus Clinical	ENSP00000317018.4:n.1480+77_1480+79del
ENST00000005226.11:c.2380+77_2380+79del	ENSP00000005226.7:n.2380+77_2380+79del
ENST00000318024.8:c.1480+77_1480+79del	ENSP00000317018.4:n.1480+77_1480+79del
ENST00000526313.5:c.*194+77_*194+79del	ENSP00000432236.1:n.*194+77_*194+79del
ENST00000527020.5:c.1423+77_1423+79del	ENSP00000436934.1:n.1423+77_1423+79del
ENST00000527720.5:c.1387+77_1387+79del	ENSP00000432944.1:n.1387+77_1387+79del
ENST00000529563.5:n.364+77_364+79del
NM_001297764.1:c.1423+77_1423+79del	NP_001284693.1:n.1423+77_1423+79del
NM_005709.3:c.1480+77_1480+79del	NP_005700.2:n.1480+77_1480+79del
NM_153676.3:c.2380+77_2380+79del	NP_710142.1:n.2380+77_2380+79del
NR_123738.1:n.1515+77_1515+79del
XM_011519831.1:c.2404+77_2404+79del	XP_011518133.1:n.2404+77_2404+79del
XM_011519832.1:c.1633+77_1633+79del	XP_011518134.1:n.1633+77_1633+79del
XM_011519832.3:c.1633+77_1633+79del	XP_011518134.1:n.1633+77_1633+79del
XM_017017075.1:c.2380+77_2380+79del	XP_016872564.1:n.2380+77_2380+79del
XR_001747717.2:n.1639+77_1639+79del
NM_153676.4:c.2380+77_2380+79del MANE Select	NP_710142.1:n.2380+77_2380+79del
NM_001297764.2:c.1423+77_1423+79del	NP_001284693.1:n.1423+77_1423+79del
NM_005709.4:c.1480+77_1480+79del MANE Plus Clinical	NP_005700.2:n.1480+77_1480+79del
NR_123738.2:n.1515+77_1515+79del