Canonical Allele Identifier: CA1141716302
Gene: USH2A HGNC NCBI

Genomic Alleles

HGVS Genome Assembly
NC_000001.11:g.215675187T= , CM000663.2:g.215675187T= GRCh38
NC_000001.10:g.215848529T= , CM000663.1:g.215848529T= GRCh37
NC_000001.9:g.213915152T= NCBI36
NG_009497.1:g.753210A=
NG_009497.2:g.753262A=

Transcript Alleles

HGVS Amino-acid Change
ENST00000307340.8:c.12724A= MANE Select ENSP00000305941.3:p.Thr4242=
ENST00000674083.1:c.12724A= ENSP00000501296.1:p.Thr4242=
ENST00000307340.7:c.12724A= ENSP00000305941.3:p.Thr4242=
NM_206933.2:c.12724A= NP_996816.2:p.Thr4242=
NM_206933.3:c.12724A= NP_996816.2:p.Thr4242=
NM_206933.4:c.12724A= MANE Select NP_996816.3:p.Thr4242=