Canonical Allele Identifier: CA1220373980
Gene: USH2A HGNC NCBI

Genomic Alleles

HGVS Genome Assembly
NC_000001.11:g.215675559_215675560delinsGA , CM000663.2:g.215675559_215675560delinsGA GRCh38
NC_000001.10:g.215848901_215848902delinsGA , CM000663.1:g.215848901_215848902delinsGA GRCh37
NC_000001.9:g.213915524_213915525delinsGA NCBI36
NG_009497.1:g.752837_752838delinsTC
NG_009497.2:g.752889_752890delinsTC

Transcript Alleles

HGVS Amino-acid Change
ENST00000307340.8:c.12351_12352delinsTC MANE Select ENSP00000305941.3:p.Phe4117=
ENST00000674083.1:c.12351_12352delinsTC ENSP00000501296.1:p.Phe4117=
ENST00000307340.7:c.12351_12352delinsTC ENSP00000305941.3:p.Phe4117=
NM_206933.2:c.12351_12352delinsTC NP_996816.2:p.Phe4117=
NM_206933.3:c.12351_12352delinsTC NP_996816.2:p.Phe4117=
NM_206933.4:c.12351_12352delinsTC MANE Select NP_996816.3:p.Phe4117=