Canonical Allele Identifier: CA2747717720
Gene: USH2A HGNC NCBI

Genomic Alleles

HGVS Genome Assembly
NC_000001.11:g.215675675dup , CM000663.2:g.215675675dup GRCh38
NC_000001.10:g.215849017dup , CM000663.1:g.215849017dup GRCh37
NC_000001.9:g.213915640dup NCBI36
NG_009497.1:g.752722dup
NG_009497.2:g.752774dup

Transcript Alleles

HGVS Amino-acid Change
ENST00000307340.8:c.12295-59dup MANE Select ENSP00000305941.3:n.12295-59dup
ENST00000674083.1:c.12295-59dup ENSP00000501296.1:n.12295-59dup
ENST00000307340.7:c.12295-59dup ENSP00000305941.3:n.12295-59dup
NM_206933.2:c.12295-59dup NP_996816.2:n.12295-59dup
NM_206933.3:c.12295-59dup NP_996816.2:n.12295-59dup
NM_206933.4:c.12295-59dup MANE Select NP_996816.3:n.12295-59dup