Canonical Allele Identifier: CA2650498173

Gene: USH2A

Linked Data

• gnomAD v4: 1-215640840-C-CAAACCAAACCAACCA

Genomic Alleles

HGVS	Genome Assembly
NC_000001.11:g.215640844_215640845insCAAACCAACCAAAAC , CM000663.2:g.215640844_215640845insCAAACCAACCAAAAC	GRCh38
NC_000001.10:g.215814186_215814187insCAAACCAACCAAAAC , CM000663.1:g.215814186_215814187insCAAACCAACCAAAAC	GRCh37
NC_000001.9:g.213880809_213880810insCAAACCAACCAAAAC	NCBI36
NG_009497.1:g.787556_787557insTGGTTGGTTTGGTTT
NG_009497.2:g.787608_787609insTGGTTGGTTTGGTTT

Transcript Alleles

HGVS	Amino-acid Change
ENST00000307340.8:c.14792-107_14792-106insTGGTTGGTTTGGTTT MANE Select	ENSP00000305941.3:n.14792-107_14792-106insTGGTTGGTTTGGTTT
ENST00000674083.1:c.14792-107_14792-106insTGGTTGGTTTGGTTT	ENSP00000501296.1:n.14792-107_14792-106insTGGTTGGTTTGGTTT
ENST00000307340.7:c.14792-107_14792-106insTGGTTGGTTTGGTTT	ENSP00000305941.3:n.14792-107_14792-106insTGGTTGGTTTGGTTT
NM_206933.2:c.14792-107_14792-106insTGGTTGGTTTGGTTT	NP_996816.2:n.14792-107_14792-106insTGGTTGGTTTGGTTT
NM_206933.3:c.14792-107_14792-106insTGGTTGGTTTGGTTT	NP_996816.2:n.14792-107_14792-106insTGGTTGGTTTGGTTT
NM_206933.4:c.14792-107_14792-106insTGGTTGGTTTGGTTT MANE Select	NP_996816.3:n.14792-107_14792-106insTGGTTGGTTTGGTTT