Canonical Allele Identifier: CA2505603371

Gene: USH2A

Genomic Alleles

HGVS	Genome Assembly
NC_000001.11:g.215640862_215640863insAAAACAAAAAACACACCAAAACAAACCAAAAAAAAAAAAAAAAAAAAA , CM000663.2:g.215640862_215640863insAAAACAAAAAACACACCAAAACAAACCAAAAAAAAAAAAAAAAAAAAA	GRCh38
NC_000001.10:g.215814204_215814205insAAAACAAAAAACACACCAAAACAAACCAAAAAAAAAAAAAAAAAAAAA , CM000663.1:g.215814204_215814205insAAAACAAAAAACACACCAAAACAAACCAAAAAAAAAAAAAAAAAAAAA	GRCh37
NC_000001.9:g.213880827_213880828insAAAACAAAAAACACACCAAAACAAACCAAAAAAAAAAAAAAAAAAAAA	NCBI36
NG_009497.1:g.787552_787553insTTTGGTTTGTTTTGGTGTGTTTTTTGTTTTTTTTTTTTTTTTTTTTTT
NG_009497.2:g.787604_787605insTTTGGTTTGTTTTGGTGTGTTTTTTGTTTTTTTTTTTTTTTTTTTTTT

Transcript Alleles

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