Canonical Allele Identifier: CA1140592563
Gene: USH2A HGNC NCBI

Genomic Alleles

HGVS Genome Assembly
NC_000001.11:g.215671258_215671260delinsCCC , CM000663.2:g.215671258_215671260delinsCCC GRCh38
NC_000001.10:g.215844600_215844602delinsCCC , CM000663.1:g.215844600_215844602delinsCCC GRCh37
NC_000001.9:g.213911223_213911225delinsCCC NCBI36
NG_009497.1:g.757137_757139delinsGGG
NG_009497.2:g.757189_757191delinsGGG

Transcript Alleles

HGVS Amino-acid change
ENST00000307340.8:c.13845_13847delinsGGG MANE Select ENSP00000305941.3:p.Leu4615=
ENST00000674083.1:c.13845_13847delinsGGG ENSP00000501296.1:p.Leu4615=
ENST00000307340.7:c.13845_13847delinsGGG ENSP00000305941.3:p.Leu4615=
NM_206933.2:c.13845_13847delinsGGG NP_996816.2:p.Leu4615=
NM_206933.3:c.13845_13847delinsGGG NP_996816.2:p.Leu4615=
NM_206933.4:c.13845_13847delinsGGG MANE Select NP_996816.3:p.Leu4615=