Canonical Allele Identifier: CA2747721925
Gene: USH2A HGNC NCBI

Genomic Alleles

HGVS Genome Assembly
NC_000001.11:g.215799223_215799235del , CM000663.2:g.215799223_215799235del GRCh38
NC_000001.10:g.215972565_215972577del , CM000663.1:g.215972565_215972577del GRCh37
NC_000001.9:g.214039188_214039200del NCBI36
NG_009497.1:g.629163_629175del
NG_009497.2:g.629215_629227del

Transcript Alleles

HGVS Amino-acid Change
ENST00000307340.8:c.9740-109_9740-97del MANE Select ENSP00000305941.3:n.9740-109_9740-97del
ENST00000674083.1:c.9740-109_9740-97del ENSP00000501296.1:n.9740-109_9740-97del
ENST00000307340.7:c.9740-109_9740-97del ENSP00000305941.3:n.9740-109_9740-97del
NM_206933.2:c.9740-109_9740-97del NP_996816.2:n.9740-109_9740-97del
NM_206933.3:c.9740-109_9740-97del NP_996816.2:n.9740-109_9740-97del
NM_206933.4:c.9740-109_9740-97del MANE Select NP_996816.3:n.9740-109_9740-97del