Canonical Allele Identifier: CA2650501715
Gene: USH2A HGNC NCBI

Linked Data

Genomic Alleles

HGVS Genome Assembly
NC_000001.11:g.215728483_215728484del , CM000663.2:g.215728483_215728484del GRCh38
NC_000001.10:g.215901825_215901826del , CM000663.1:g.215901825_215901826del GRCh37
NC_000001.9:g.213968448_213968449del NCBI36
NG_009497.1:g.699913_699914del
NG_009497.2:g.699965_699966del

Transcript Alleles

HGVS Amino-acid Change
ENST00000307340.8:c.11712-100_11712-99del MANE Select ENSP00000305941.3:n.11712-100_11712-99del
ENST00000674083.1:c.11712-100_11712-99del ENSP00000501296.1:n.11712-100_11712-99del
ENST00000307340.7:c.11712-100_11712-99del ENSP00000305941.3:n.11712-100_11712-99del
NM_206933.2:c.11712-100_11712-99del NP_996816.2:n.11712-100_11712-99del
NM_206933.3:c.11712-100_11712-99del NP_996816.2:n.11712-100_11712-99del
NM_206933.4:c.11712-100_11712-99del MANE Select NP_996816.3:n.11712-100_11712-99del