Canonical Allele Identifier: CA1220396703
Gene: USH2A HGNC NCBI

Genomic Alleles

HGVS Genome Assembly
NC_000001.11:g.215728666G= , CM000663.2:g.215728666G= GRCh38
NC_000001.10:g.215902008G= , CM000663.1:g.215902008G= GRCh37
NC_000001.9:g.213968631G= NCBI36
NG_009497.1:g.699731C=
NG_009497.2:g.699783C=

Transcript Alleles

HGVS Amino-acid Change
ENST00000307340.8:c.11712-282C= MANE Select ENSP00000305941.3:n.11712-282C=
ENST00000674083.1:c.11712-282C= ENSP00000501296.1:n.11712-282C=
ENST00000307340.7:c.11712-282C= ENSP00000305941.3:n.11712-282C=
NM_206933.2:c.11712-282C= NP_996816.2:n.11712-282C=
NM_206933.3:c.11712-282C= NP_996816.2:n.11712-282C=
NM_206933.4:c.11712-282C= MANE Select NP_996816.3:n.11712-282C=