Canonical Allele Identifier: CA2790592561

Gene: USH1C

Genomic Alleles

HGVS	Genome Assembly
NC_000011.10:g.17500939_17500996del , CM000673.2:g.17500939_17500996del	GRCh38
NC_000011.9:g.17522486_17522543del , CM000673.1:g.17522486_17522543del	GRCh37
NC_000011.8:g.17479062_17479119del	NCBI36
NG_011883.1:g.48429_48486del
NG_011883.2:g.48429_48486del

Transcript Alleles

HGVS	Amino-acid Change
ENST00000005226.12:c.2380+63_2380+120del MANE Select	ENSP00000005226.7:n.2380+63_2380+120del
ENST00000318024.9:c.1480+63_1480+120del MANE Plus Clinical	ENSP00000317018.4:n.1480+63_1480+120del
ENST00000005226.11:c.2380+63_2380+120del	ENSP00000005226.7:n.2380+63_2380+120del
ENST00000318024.8:c.1480+63_1480+120del	ENSP00000317018.4:n.1480+63_1480+120del
ENST00000526313.5:c.*194+63_*194+120del	ENSP00000432236.1:n.*194+63_*194+120del
ENST00000527020.5:c.1423+63_1423+120del	ENSP00000436934.1:n.1423+63_1423+120del
ENST00000527720.5:c.1387+63_1387+120del	ENSP00000432944.1:n.1387+63_1387+120del
ENST00000529563.5:n.364+63_364+120del
NM_001297764.1:c.1423+63_1423+120del	NP_001284693.1:n.1423+63_1423+120del
NM_005709.3:c.1480+63_1480+120del	NP_005700.2:n.1480+63_1480+120del
NM_153676.3:c.2380+63_2380+120del	NP_710142.1:n.2380+63_2380+120del
NR_123738.1:n.1515+63_1515+120del
XM_011519831.1:c.2404+63_2404+120del	XP_011518133.1:n.2404+63_2404+120del
XM_011519832.1:c.1633+63_1633+120del	XP_011518134.1:n.1633+63_1633+120del
XM_011519832.3:c.1633+63_1633+120del	XP_011518134.1:n.1633+63_1633+120del
XM_017017075.1:c.2380+63_2380+120del	XP_016872564.1:n.2380+63_2380+120del
XR_001747717.2:n.1639+63_1639+120del
NM_153676.4:c.2380+63_2380+120del MANE Select	NP_710142.1:n.2380+63_2380+120del
NM_001297764.2:c.1423+63_1423+120del	NP_001284693.1:n.1423+63_1423+120del
NM_005709.4:c.1480+63_1480+120del MANE Plus Clinical	NP_005700.2:n.1480+63_1480+120del
NR_123738.2:n.1515+63_1515+120del