Canonical Allele Identifier: CA2650499200

Gene: USH2A

Linked Data

• gnomAD v4: 1-215640844-C-CAAACAAAACCAAACCAAA

Genomic Alleles

HGVS	Genome Assembly
NC_000001.11:g.215640847_215640848insCAAAACCAAACCAAAAAA , CM000663.2:g.215640847_215640848insCAAAACCAAACCAAAAAA	GRCh38
NC_000001.10:g.215814189_215814190insCAAAACCAAACCAAAAAA , CM000663.1:g.215814189_215814190insCAAAACCAAACCAAAAAA	GRCh37
NC_000001.9:g.213880812_213880813insCAAAACCAAACCAAAAAA	NCBI36
NG_009497.1:g.787552_787553insTTTGGTTTGGTTTTGTTT
NG_009497.2:g.787604_787605insTTTGGTTTGGTTTTGTTT

Transcript Alleles

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