Canonical Allele Identifier: CA2747716391
Gene: USH2A HGNC NCBI

Genomic Alleles

HGVS Genome Assembly
NC_000001.11:g.215640766_215640767insACA , CM000663.2:g.215640766_215640767insACA GRCh38
NC_000001.10:g.215814108_215814109insACA , CM000663.1:g.215814108_215814109insACA GRCh37
NC_000001.9:g.213880731_213880732insACA NCBI36
NG_009497.1:g.787630_787631insTGT
NG_009497.2:g.787682_787683insTGT

Transcript Alleles

HGVS Amino-acid Change
ENST00000307340.8:c.14792-33_14792-32insTGT MANE Select ENSP00000305941.3:n.14792-33_14792-32insTGT
ENST00000674083.1:c.14792-33_14792-32insTGT ENSP00000501296.1:n.14792-33_14792-32insTGT
ENST00000307340.7:c.14792-33_14792-32insTGT ENSP00000305941.3:n.14792-33_14792-32insTGT
NM_206933.2:c.14792-33_14792-32insTGT NP_996816.2:n.14792-33_14792-32insTGT
NM_206933.3:c.14792-33_14792-32insTGT NP_996816.2:n.14792-33_14792-32insTGT
NM_206933.4:c.14792-33_14792-32insTGT MANE Select NP_996816.3:n.14792-33_14792-32insTGT