Canonical Allele Identifier: CA1220434331
Gene: USH2A HGNC NCBI

Genomic Alleles

HGVS Genome Assembly
NC_000001.11:g.215817103T= , CM000663.2:g.215817103T= GRCh38
NC_000001.10:g.215990445T= , CM000663.1:g.215990445T= GRCh37
NC_000001.9:g.214057068T= NCBI36
NG_009497.1:g.611294A=
NG_009497.2:g.611346A=

Transcript Alleles

HGVS Amino-acid Change
ENST00000307340.8:c.9464A= MANE Select ENSP00000305941.3:p.Lys3155=
ENST00000674083.1:c.9464A= ENSP00000501296.1:p.Lys3155=
ENST00000307340.7:c.9464A= ENSP00000305941.3:p.Lys3155=
NM_206933.2:c.9464A= NP_996816.2:p.Lys3155=
NM_206933.3:c.9464A= NP_996816.2:p.Lys3155=
NM_206933.4:c.9464A= MANE Select NP_996816.3:p.Lys3155=