Canonical Allele Identifier: CA2790591837
Gene: USH1C HGNC NCBI

Genomic Alleles

HGVS Genome Assembly
NC_000011.10:g.17494470_17494471insG , CM000673.2:g.17494470_17494471insG GRCh38
NC_000011.9:g.17516017_17516018insG , CM000673.1:g.17516017_17516018insG GRCh37
NC_000011.8:g.17472593_17472594insG NCBI36
NG_011883.1:g.54946_54947insC
NG_011883.2:g.54946_54947insC

Transcript Alleles

HGVS Amino-acid Change
ENST00000005226.12:c.2656-95_2656-94insC MANE Select ENSP00000005226.7:n.2656-95_2656-94insC
ENST00000318024.9:c.1647-95_1647-94insC MANE Plus Clinical ENSP00000317018.4:n.1647-95_1647-94insC
ENST00000005226.11:c.2656-95_2656-94insC ENSP00000005226.7:n.2656-95_2656-94insC
ENST00000318024.8:c.1647-95_1647-94insC ENSP00000317018.4:n.1647-95_1647-94insC
ENST00000526313.5:c.*361-95_*361-94insC ENSP00000432236.1:n.*361-95_*361-94insC
ENST00000527020.5:c.1590-95_1590-94insC ENSP00000436934.1:n.1590-95_1590-94insC
ENST00000527551.1:n.157-95_157-94insC
ENST00000527720.5:c.1554-95_1554-94insC ENSP00000432944.1:n.1554-95_1554-94insC
ENST00000529563.5:n.531-95_531-94insC
ENST00000624811.1:n.623_624insC
NM_001297764.1:c.1590-95_1590-94insC NP_001284693.1:n.1590-95_1590-94insC
NM_005709.3:c.1647-95_1647-94insC NP_005700.2:n.1647-95_1647-94insC
NM_153676.3:c.2656-95_2656-94insC NP_710142.1:n.2656-95_2656-94insC
NR_123738.1:n.1682-95_1682-94insC
XM_011519831.1:c.2571-95_2571-94insC XP_011518133.1:n.2571-95_2571-94insC
XM_011519832.1:c.1800-95_1800-94insC XP_011518134.1:n.1800-95_1800-94insC
XM_011519832.3:c.1800-95_1800-94insC XP_011518134.1:n.1800-95_1800-94insC
XM_017017075.1:c.*882_*883insC XP_016872564.1:n.*882_*883insC
XR_001747717.2:n.1806-95_1806-94insC
NM_153676.4:c.2656-95_2656-94insC MANE Select NP_710142.1:n.2656-95_2656-94insC
NM_001297764.2:c.1590-95_1590-94insC NP_001284693.1:n.1590-95_1590-94insC
NM_005709.4:c.1647-95_1647-94insC MANE Plus Clinical NP_005700.2:n.1647-95_1647-94insC
NR_123738.2:n.1682-95_1682-94insC