Canonical Allele Identifier: CA2650500789
Gene: USH2A HGNC NCBI

Linked Data

Genomic Alleles

HGVS Genome Assembly
NC_000001.11:g.215675696del , CM000663.2:g.215675696del GRCh38
NC_000001.10:g.215849038del , CM000663.1:g.215849038del GRCh37
NC_000001.9:g.213915661del NCBI36
NG_009497.1:g.752701del
NG_009497.2:g.752753del

Transcript Alleles

HGVS Amino-acid Change
ENST00000307340.8:c.12295-80del MANE Select ENSP00000305941.3:n.12295-80del
ENST00000674083.1:c.12295-80del ENSP00000501296.1:n.12295-80del
ENST00000307340.7:c.12295-80del ENSP00000305941.3:n.12295-80del
NM_206933.2:c.12295-80del NP_996816.2:n.12295-80del
NM_206933.3:c.12295-80del NP_996816.2:n.12295-80del
NM_206933.4:c.12295-80del MANE Select NP_996816.3:n.12295-80del