Canonical Allele Identifier: CA1143547210
Gene: USH2A HGNC NCBI

Genomic Alleles

HGVS Genome Assembly
NC_000001.11:g.215671283G= , CM000663.2:g.215671283G= GRCh38
NC_000001.10:g.215844625G= , CM000663.1:g.215844625G= GRCh37
NC_000001.9:g.213911248G= NCBI36
NG_009497.1:g.757114C=
NG_009497.2:g.757166C=

Transcript Alleles

HGVS Amino-acid Change
ENST00000307340.8:c.13822C= MANE Select ENSP00000305941.3:p.Arg4608=
ENST00000674083.1:c.13822C= ENSP00000501296.1:p.Arg4608=
ENST00000307340.7:c.13822C= ENSP00000305941.3:p.Arg4608=
NM_206933.2:c.13822C= NP_996816.2:p.Arg4608=
NM_206933.3:c.13822C= NP_996816.2:p.Arg4608=
NM_206933.4:c.13822C= MANE Select NP_996816.3:p.Arg4608=