Canonical Allele Identifier: CA2747716456
Gene: USH2A HGNC NCBI

Genomic Alleles

HGVS Genome Assembly
NC_000001.11:g.215640797_215640798insAGA , CM000663.2:g.215640797_215640798insAGA GRCh38
NC_000001.10:g.215814139_215814140insAGA , CM000663.1:g.215814139_215814140insAGA GRCh37
NC_000001.9:g.213880762_213880763insAGA NCBI36
NG_009497.1:g.787599_787600insTCT
NG_009497.2:g.787651_787652insTCT

Transcript Alleles

HGVS Amino-acid Change
ENST00000307340.8:c.14792-64_14792-63insTCT MANE Select ENSP00000305941.3:n.14792-64_14792-63insTCT
ENST00000674083.1:c.14792-64_14792-63insTCT ENSP00000501296.1:n.14792-64_14792-63insTCT
ENST00000307340.7:c.14792-64_14792-63insTCT ENSP00000305941.3:n.14792-64_14792-63insTCT
NM_206933.2:c.14792-64_14792-63insTCT NP_996816.2:n.14792-64_14792-63insTCT
NM_206933.3:c.14792-64_14792-63insTCT NP_996816.2:n.14792-64_14792-63insTCT
NM_206933.4:c.14792-64_14792-63insTCT MANE Select NP_996816.3:n.14792-64_14792-63insTCT