Canonical Allele Identifier: CA2612670461

Gene: USH1C

Linked Data

• gnomAD v4: 11-17494577-CGGGAGGGACACCTGGGATGGGGGAAGGAGGAGACT-C

Genomic Alleles

HGVS	Genome Assembly
NC_000011.10:g.17494584_17494618del , CM000673.2:g.17494584_17494618del	GRCh38
NC_000011.9:g.17516131_17516165del , CM000673.1:g.17516131_17516165del	GRCh37
NC_000011.8:g.17472707_17472741del	NCBI36
NG_011883.1:g.54805_54839del
NG_011883.2:g.54805_54839del

Transcript Alleles

HGVS	Amino-acid Change
ENST00000005226.12:c.2656-236_2656-202del MANE Select	ENSP00000005226.7:n.2656-236_2656-202del
ENST00000318024.9:c.1647-236_1647-202del MANE Plus Clinical	ENSP00000317018.4:n.1647-236_1647-202del
ENST00000005226.11:c.2656-236_2656-202del	ENSP00000005226.7:n.2656-236_2656-202del
ENST00000318024.8:c.1647-236_1647-202del	ENSP00000317018.4:n.1647-236_1647-202del
ENST00000526313.5:c.*361-236_*361-202del	ENSP00000432236.1:n.*361-236_*361-202del
ENST00000527020.5:c.1590-236_1590-202del	ENSP00000436934.1:n.1590-236_1590-202del
ENST00000527551.1:n.157-236_157-202del
ENST00000527720.5:c.1554-236_1554-202del	ENSP00000432944.1:n.1554-236_1554-202del
ENST00000529563.5:n.531-236_531-202del
ENST00000624811.1:n.482_516del
NM_001297764.1:c.1590-236_1590-202del	NP_001284693.1:n.1590-236_1590-202del
NM_005709.3:c.1647-236_1647-202del	NP_005700.2:n.1647-236_1647-202del
NM_153676.3:c.2656-236_2656-202del	NP_710142.1:n.2656-236_2656-202del
NR_123738.1:n.1682-236_1682-202del
XM_011519831.1:c.2571-236_2571-202del	XP_011518133.1:n.2571-236_2571-202del
XM_011519832.1:c.1800-236_1800-202del	XP_011518134.1:n.1800-236_1800-202del
XM_011519832.3:c.1800-236_1800-202del	XP_011518134.1:n.1800-236_1800-202del
XM_017017075.1:c.*741_*775del	XP_016872564.1:n.*741_*775del
XR_001747717.2:n.1806-236_1806-202del
NM_153676.4:c.2656-236_2656-202del MANE Select	NP_710142.1:n.2656-236_2656-202del
NM_001297764.2:c.1590-236_1590-202del	NP_001284693.1:n.1590-236_1590-202del
NM_005709.4:c.1647-236_1647-202del MANE Plus Clinical	NP_005700.2:n.1647-236_1647-202del
NR_123738.2:n.1682-236_1682-202del