Canonical Allele Identifier: CA2747719157
Gene: USH2A HGNC NCBI

Genomic Alleles

HGVS Genome Assembly
NC_000001.11:g.215728529_215728530insAACACACCCAACACA , CM000663.2:g.215728529_215728530insAACACACCCAACACA GRCh38
NC_000001.10:g.215901871_215901872insAACACACCCAACACA , CM000663.1:g.215901871_215901872insAACACACCCAACACA GRCh37
NC_000001.9:g.213968494_213968495insAACACACCCAACACA NCBI36
NG_009497.1:g.699869_699870insTGTTGGGTGTGTTTG
NG_009497.2:g.699921_699922insTGTTGGGTGTGTTTG

Transcript Alleles

HGVS Amino-acid Change
ENST00000307340.8:c.11712-144_11712-143insTGTTGGGTGTGTTTG MANE Select ENSP00000305941.3:n.11712-144_11712-143insTGTTGGGTGTGTTTG
ENST00000674083.1:c.11712-144_11712-143insTGTTGGGTGTGTTTG ENSP00000501296.1:n.11712-144_11712-143insTGTTGGGTGTGTTTG
ENST00000307340.7:c.11712-144_11712-143insTGTTGGGTGTGTTTG ENSP00000305941.3:n.11712-144_11712-143insTGTTGGGTGTGTTTG
NM_206933.2:c.11712-144_11712-143insTGTTGGGTGTGTTTG NP_996816.2:n.11712-144_11712-143insTGTTGGGTGTGTTTG
NM_206933.3:c.11712-144_11712-143insTGTTGGGTGTGTTTG NP_996816.2:n.11712-144_11712-143insTGTTGGGTGTGTTTG
NM_206933.4:c.11712-144_11712-143insTGTTGGGTGTGTTTG MANE Select NP_996816.3:n.11712-144_11712-143insTGTTGGGTGTGTTTG