Canonical Allele Identifier: CA1012185148

Gene: USH2A

Linked Data

• dbSNP Id: rs56212994
• gnomAD v3: 1-215640844-C-CAAAAAAAAAAAAAAAAAAAAAACAAACCGAACCAAACCAAAA
• gnomAD v4: 1-215640844-C-CAAAAAAAAAAAAAAAAAAAAAACAAACCGAACCAAACCAAAA

Genomic Alleles

HGVS	Genome Assembly
NC_000001.11:g.215640862_215640863insAAAACAAACCGAACCAAACCAAAAAAAAAAAAAAAAAAAAAA , CM000663.2:g.215640862_215640863insAAAACAAACCGAACCAAACCAAAAAAAAAAAAAAAAAAAAAA	GRCh38
NC_000001.10:g.215814204_215814205insAAAACAAACCGAACCAAACCAAAAAAAAAAAAAAAAAAAAAA , CM000663.1:g.215814204_215814205insAAAACAAACCGAACCAAACCAAAAAAAAAAAAAAAAAAAAAA	GRCh37
NC_000001.9:g.213880827_213880828insAAAACAAACCGAACCAAACCAAAAAAAAAAAAAAAAAAAAAA	NCBI36
NG_009497.1:g.787552_787553insTTTTGGTTTGGTTCGGTTTGTTTTTTTTTTTTTTTTTTTTTT
NG_009497.2:g.787604_787605insTTTTGGTTTGGTTCGGTTTGTTTTTTTTTTTTTTTTTTTTTT

Transcript Alleles

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