Canonical Allele Identifier: CA2650498110

Gene: USH2A

Linked Data

• gnomAD v4: 1-215640799-T-TA

Genomic Alleles

HGVS	Genome Assembly
NC_000001.11:g.215640799_215640800insA , CM000663.2:g.215640799_215640800insA	GRCh38
NC_000001.10:g.215814141_215814142insA , CM000663.1:g.215814141_215814142insA	GRCh37
NC_000001.9:g.213880764_213880765insA	NCBI36
NG_009497.1:g.787597_787598insT
NG_009497.2:g.787649_787650insT

Transcript Alleles

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