Canonical Allele Identifier: CA2612670418

Gene: USH1C

Linked Data

• gnomAD v4: 11-17494538-CCAGCCA-C

Genomic Alleles

HGVS	Genome Assembly
NC_000011.10:g.17494549_17494554del , CM000673.2:g.17494549_17494554del	GRCh38
NC_000011.9:g.17516096_17516101del , CM000673.1:g.17516096_17516101del	GRCh37
NC_000011.8:g.17472672_17472677del	NCBI36
NG_011883.1:g.54873_54878del
NG_011883.2:g.54873_54878del

Transcript Alleles

HGVS	Amino-acid Change
ENST00000005226.12:c.2656-168_2656-163del MANE Select	ENSP00000005226.7:n.2656-168_2656-163del
ENST00000318024.9:c.1647-168_1647-163del MANE Plus Clinical	ENSP00000317018.4:n.1647-168_1647-163del
ENST00000005226.11:c.2656-168_2656-163del	ENSP00000005226.7:n.2656-168_2656-163del
ENST00000318024.8:c.1647-168_1647-163del	ENSP00000317018.4:n.1647-168_1647-163del
ENST00000526313.5:c.*361-168_*361-163del	ENSP00000432236.1:n.*361-168_*361-163del
ENST00000527020.5:c.1590-168_1590-163del	ENSP00000436934.1:n.1590-168_1590-163del
ENST00000527551.1:n.157-168_157-163del
ENST00000527720.5:c.1554-168_1554-163del	ENSP00000432944.1:n.1554-168_1554-163del
ENST00000529563.5:n.531-168_531-163del
ENST00000624811.1:n.550_555del
NM_001297764.1:c.1590-168_1590-163del	NP_001284693.1:n.1590-168_1590-163del
NM_005709.3:c.1647-168_1647-163del	NP_005700.2:n.1647-168_1647-163del
NM_153676.3:c.2656-168_2656-163del	NP_710142.1:n.2656-168_2656-163del
NR_123738.1:n.1682-168_1682-163del
XM_011519831.1:c.2571-168_2571-163del	XP_011518133.1:n.2571-168_2571-163del
XM_011519832.1:c.1800-168_1800-163del	XP_011518134.1:n.1800-168_1800-163del
XM_011519832.3:c.1800-168_1800-163del	XP_011518134.1:n.1800-168_1800-163del
XM_017017075.1:c.*809_*814del	XP_016872564.1:n.*809_*814del
XR_001747717.2:n.1806-168_1806-163del
NM_153676.4:c.2656-168_2656-163del MANE Select	NP_710142.1:n.2656-168_2656-163del
NM_001297764.2:c.1590-168_1590-163del	NP_001284693.1:n.1590-168_1590-163del
NM_005709.4:c.1647-168_1647-163del MANE Plus Clinical	NP_005700.2:n.1647-168_1647-163del
NR_123738.2:n.1682-168_1682-163del