Canonical Allele Identifier: CA2747716465
Gene: USH2A HGNC NCBI

Genomic Alleles

HGVS Genome Assembly
NC_000001.11:g.215640799_215640800insACG , CM000663.2:g.215640799_215640800insACG GRCh38
NC_000001.10:g.215814141_215814142insACG , CM000663.1:g.215814141_215814142insACG GRCh37
NC_000001.9:g.213880764_213880765insACG NCBI36
NG_009497.1:g.787597_787598insCGT
NG_009497.2:g.787649_787650insCGT

Transcript Alleles

HGVS Amino-acid Change
ENST00000307340.8:c.14792-66_14792-65insCGT MANE Select ENSP00000305941.3:n.14792-66_14792-65insCGT
ENST00000674083.1:c.14792-66_14792-65insCGT ENSP00000501296.1:n.14792-66_14792-65insCGT
ENST00000307340.7:c.14792-66_14792-65insCGT ENSP00000305941.3:n.14792-66_14792-65insCGT
NM_206933.2:c.14792-66_14792-65insCGT NP_996816.2:n.14792-66_14792-65insCGT
NM_206933.3:c.14792-66_14792-65insCGT NP_996816.2:n.14792-66_14792-65insCGT
NM_206933.4:c.14792-66_14792-65insCGT MANE Select NP_996816.3:n.14792-66_14792-65insCGT