Canonical Allele Identifier: CA2747721940
Gene: USH2A HGNC NCBI

Genomic Alleles

HGVS Genome Assembly
NC_000001.11:g.215799234_215799235insA , CM000663.2:g.215799234_215799235insA GRCh38
NC_000001.10:g.215972576_215972577insA , CM000663.1:g.215972576_215972577insA GRCh37
NC_000001.9:g.214039199_214039200insA NCBI36
NG_009497.1:g.629162_629163insT
NG_009497.2:g.629214_629215insT

Transcript Alleles

HGVS Amino-acid Change
ENST00000307340.8:c.9740-110_9740-109insT MANE Select ENSP00000305941.3:n.9740-110_9740-109insT
ENST00000674083.1:c.9740-110_9740-109insT ENSP00000501296.1:n.9740-110_9740-109insT
ENST00000307340.7:c.9740-110_9740-109insT ENSP00000305941.3:n.9740-110_9740-109insT
NM_206933.2:c.9740-110_9740-109insT NP_996816.2:n.9740-110_9740-109insT
NM_206933.3:c.9740-110_9740-109insT NP_996816.2:n.9740-110_9740-109insT
NM_206933.4:c.9740-110_9740-109insT MANE Select NP_996816.3:n.9740-110_9740-109insT