Canonical Allele Identifier: CA1220396651
Gene: USH2A HGNC NCBI

Genomic Alleles

HGVS Genome Assembly
NC_000001.11:g.215728552_215728560delinsCTAACTCCA , CM000663.2:g.215728552_215728560delinsCTAACTCCA GRCh38
NC_000001.10:g.215901894_215901902delinsCTAACTCCA , CM000663.1:g.215901894_215901902delinsCTAACTCCA GRCh37
NC_000001.9:g.213968517_213968525delinsCTAACTCCA NCBI36
NG_009497.1:g.699837_699845delinsTGGAGTTAG
NG_009497.2:g.699889_699897delinsTGGAGTTAG

Transcript Alleles

HGVS Amino-acid Change
ENST00000307340.8:c.11712-176_11712-168delinsTGGAGTTAG MANE Select ENSP00000305941.3:n.11712-176_11712-168delinsTGGAGTTAG
ENST00000674083.1:c.11712-176_11712-168delinsTGGAGTTAG ENSP00000501296.1:n.11712-176_11712-168delinsTGGAGTTAG
ENST00000307340.7:c.11712-176_11712-168delinsTGGAGTTAG ENSP00000305941.3:n.11712-176_11712-168delinsTGGAGTTAG
NM_206933.2:c.11712-176_11712-168delinsTGGAGTTAG NP_996816.2:n.11712-176_11712-168delinsTGGAGTTAG
NM_206933.3:c.11712-176_11712-168delinsTGGAGTTAG NP_996816.2:n.11712-176_11712-168delinsTGGAGTTAG
NM_206933.4:c.11712-176_11712-168delinsTGGAGTTAG MANE Select NP_996816.3:n.11712-176_11712-168delinsTGGAGTTAG