Canonical Allele Identifier: CA2650499366

Gene: USH2A

Linked Data

• gnomAD v4: 1-215640844-C-CAAAAAAAAAAAAAAAAAAAAAAAAACAAAACAATCCAAA

Genomic Alleles

HGVS	Genome Assembly
NC_000001.11:g.215640862_215640863insAAAAAAACAAAACAATCCAAAAAAAAAAAAAAAAAAAAA , CM000663.2:g.215640862_215640863insAAAAAAACAAAACAATCCAAAAAAAAAAAAAAAAAAAAA	GRCh38
NC_000001.10:g.215814204_215814205insAAAAAAACAAAACAATCCAAAAAAAAAAAAAAAAAAAAA , CM000663.1:g.215814204_215814205insAAAAAAACAAAACAATCCAAAAAAAAAAAAAAAAAAAAA	GRCh37
NC_000001.9:g.213880827_213880828insAAAAAAACAAAACAATCCAAAAAAAAAAAAAAAAAAAAA	NCBI36
NG_009497.1:g.787552_787553insTTTGGATTGTTTTGTTTTTTTTTTTTTTTTTTTTTTTTT
NG_009497.2:g.787604_787605insTTTGGATTGTTTTGTTTTTTTTTTTTTTTTTTTTTTTTT

Transcript Alleles

HGVS	Amino-acid Change
ENST00000307340.8:c.14792-111_14792-110insTTTGGATTGTTTTGTTTTTTTTTTTTTTTTTTTTTTTTT MANE Select	ENSP00000305941.3:n.14792-111_14792-110insTTTGGATTGTTTTGTTTTT...
ENST00000674083.1:c.14792-111_14792-110insTTTGGATTGTTTTGTTTTTTTTTTTTTTTTTTTTTTTTT	ENSP00000501296.1:n.14792-111_14792-110insTTTGGATTGTTTTGTTTTT...
ENST00000307340.7:c.14792-111_14792-110insTTTGGATTGTTTTGTTTTTTTTTTTTTTTTTTTTTTTTT	ENSP00000305941.3:n.14792-111_14792-110insTTTGGATTGTTTTGTTTTT...
NM_206933.2:c.14792-111_14792-110insTTTGGATTGTTTTGTTTTTTTTTTTTTTTTTTTTTTTTT	NP_996816.2:n.14792-111_14792-110insTTTGGATTGTTTTGTTTTTTTTTTT...
NM_206933.3:c.14792-111_14792-110insTTTGGATTGTTTTGTTTTTTTTTTTTTTTTTTTTTTTTT	NP_996816.2:n.14792-111_14792-110insTTTGGATTGTTTTGTTTTTTTTTTT...
NM_206933.4:c.14792-111_14792-110insTTTGGATTGTTTTGTTTTTTTTTTTTTTTTTTTTTTTTT MANE Select	NP_996816.3:n.14792-111_14792-110insTTTGGATTGTTTTGTTTTTTTTTTT...