Canonical Allele Identifier: CA916402634
Gene: USH2A HGNC NCBI

Linked Data

dbSNP Id: rs1571627233

Genomic Alleles

HGVS Genome Assembly
NC_000001.11:g.215728617_215728619dup , CM000663.2:g.215728617_215728619dup GRCh38
NC_000001.10:g.215901959_215901961dup , CM000663.1:g.215901959_215901961dup GRCh37
NC_000001.9:g.213968582_213968584dup NCBI36
NG_009497.1:g.699779_699781dup
NG_009497.2:g.699831_699833dup

Transcript Alleles

HGVS Amino-acid Change
ENST00000307340.8:c.11712-234_11712-232dup MANE Select ENSP00000305941.3:n.11712-234_11712-232dup
ENST00000674083.1:c.11712-234_11712-232dup ENSP00000501296.1:n.11712-234_11712-232dup
ENST00000307340.7:c.11712-234_11712-232dup ENSP00000305941.3:n.11712-234_11712-232dup
NM_206933.2:c.11712-234_11712-232dup NP_996816.2:n.11712-234_11712-232dup
NM_206933.3:c.11712-234_11712-232dup NP_996816.2:n.11712-234_11712-232dup
NM_206933.4:c.11712-234_11712-232dup MANE Select NP_996816.3:n.11712-234_11712-232dup