Canonical Allele Identifier: CA1220396558
Gene: USH2A HGNC NCBI

Genomic Alleles

HGVS Genome Assembly
NC_000001.11:g.215728283_215728285delinsTAG , CM000663.2:g.215728283_215728285delinsTAG GRCh38
NC_000001.10:g.215901625_215901627delinsTAG , CM000663.1:g.215901625_215901627delinsTAG GRCh37
NC_000001.9:g.213968248_213968250delinsTAG NCBI36
NG_009497.1:g.700112_700114delinsCTA
NG_009497.2:g.700164_700166delinsCTA

Transcript Alleles

HGVS Amino-acid Change
ENST00000307340.8:c.11811_11813delinsCTA MANE Select ENSP00000305941.3:p.Leu3937=
ENST00000674083.1:c.11811_11813delinsCTA ENSP00000501296.1:p.Leu3937=
ENST00000307340.7:c.11811_11813delinsCTA ENSP00000305941.3:p.Leu3937=
NM_206933.2:c.11811_11813delinsCTA NP_996816.2:p.Leu3937=
NM_206933.3:c.11811_11813delinsCTA NP_996816.2:p.Leu3937=
NM_206933.4:c.11811_11813delinsCTA MANE Select NP_996816.3:p.Leu3937=