Canonical Allele Identifier: CA1220619217
Gene: USH2A HGNC NCBI

Genomic Alleles

HGVS Genome Assembly
NC_000001.11:g.216247014C= , CM000663.2:g.216247014C= GRCh38
NC_000001.10:g.216420356C= , CM000663.1:g.216420356C= GRCh37
NC_000001.9:g.214486979C= NCBI36
NG_009497.1:g.181383G=
NG_009497.2:g.181435G=

Transcript Alleles

HGVS Amino-acid Change
ENST00000307340.8:c.2380G= MANE Select ENSP00000305941.3:p.Ala794=
ENST00000674083.1:c.2380G= ENSP00000501296.1:p.Ala794=
ENST00000307340.7:c.2380G= ENSP00000305941.3:p.Ala794=
ENST00000366942.3:c.2380G= ENSP00000355909.3:p.Ala794=
NM_007123.5:c.2380G= NP_009054.5:p.Ala794=
NM_206933.2:c.2380G= NP_996816.2:p.Ala794=
NM_206933.3:c.2380G= NP_996816.2:p.Ala794=
NM_007123.6:c.2380G= NP_009054.6:p.Ala794=
NM_206933.4:c.2380G= MANE Select NP_996816.3:p.Ala794=