Canonical Allele Identifier: CA731341604
Gene: USH2A HGNC NCBI

Linked Data

dbSNP Id: rs1478897080

Genomic Alleles

HGVS Genome Assembly
NC_000001.11:g.215728007_215728012dup , CM000663.2:g.215728007_215728012dup GRCh38
NC_000001.10:g.215901349_215901354dup , CM000663.1:g.215901349_215901354dup GRCh37
NC_000001.9:g.213967972_213967977dup NCBI36
NG_009497.1:g.700387_700392dup
NG_009497.2:g.700439_700444dup

Transcript Alleles

HGVS Amino-acid Change
ENST00000307340.8:c.12066+20_12066+25dup MANE Select ENSP00000305941.3:n.12066+20_12066+25dup
ENST00000674083.1:c.12066+20_12066+25dup ENSP00000501296.1:n.12066+20_12066+25dup
ENST00000307340.7:c.12066+20_12066+25dup ENSP00000305941.3:n.12066+20_12066+25dup
NM_206933.2:c.12066+20_12066+25dup NP_996816.2:n.12066+20_12066+25dup
NM_206933.3:c.12066+20_12066+25dup NP_996816.2:n.12066+20_12066+25dup
NM_206933.4:c.12066+20_12066+25dup MANE Select NP_996816.3:n.12066+20_12066+25dup