Canonical Allele Identifier: CA1148870465
Gene: USH2A HGNC NCBI

Genomic Alleles

HGVS Genome Assembly
NC_000001.11:g.215728459_215728466delinsTTTTTTTT , CM000663.2:g.215728459_215728466delinsTTTTTTTT GRCh38
NC_000001.10:g.215901801_215901808delinsTTTTTTTT , CM000663.1:g.215901801_215901808delinsTTTTTTTT GRCh37
NC_000001.9:g.213968424_213968431delinsTTTTTTTT NCBI36
NG_009497.1:g.699931_699938delinsAAAAAAAA
NG_009497.2:g.699983_699990delinsAAAAAAAA

Transcript Alleles

HGVS Amino-acid Change
ENST00000307340.8:c.11712-82_11712-75delinsAAAAAAAA MANE Select ENSP00000305941.3:n.11712-82_11712-75delinsAAAAAAAA
ENST00000674083.1:c.11712-82_11712-75delinsAAAAAAAA ENSP00000501296.1:n.11712-82_11712-75delinsAAAAAAAA
ENST00000307340.7:c.11712-82_11712-75delinsAAAAAAAA ENSP00000305941.3:n.11712-82_11712-75delinsAAAAAAAA
NM_206933.2:c.11712-82_11712-75delinsAAAAAAAA NP_996816.2:n.11712-82_11712-75delinsAAAAAAAA
NM_206933.3:c.11712-82_11712-75delinsAAAAAAAA NP_996816.2:n.11712-82_11712-75delinsAAAAAAAA
NM_206933.4:c.11712-82_11712-75delinsAAAAAAAA MANE Select NP_996816.3:n.11712-82_11712-75delinsAAAAAAAA