Canonical Allele Identifier: CA2747716500

Gene: USH2A

Genomic Alleles

HGVS	Genome Assembly
NC_000001.11:g.215640830_215640831insACTG , CM000663.2:g.215640830_215640831insACTG	GRCh38
NC_000001.10:g.215814172_215814173insACTG , CM000663.1:g.215814172_215814173insACTG	GRCh37
NC_000001.9:g.213880795_213880796insACTG	NCBI36
NG_009497.1:g.787566_787567insCAGT
NG_009497.2:g.787618_787619insCAGT

Transcript Alleles

HGVS	Amino-acid Change
ENST00000307340.8:c.14792-97_14792-96insCAGT MANE Select	ENSP00000305941.3:n.14792-97_14792-96insCAGT
ENST00000674083.1:c.14792-97_14792-96insCAGT	ENSP00000501296.1:n.14792-97_14792-96insCAGT
ENST00000307340.7:c.14792-97_14792-96insCAGT	ENSP00000305941.3:n.14792-97_14792-96insCAGT
NM_206933.2:c.14792-97_14792-96insCAGT	NP_996816.2:n.14792-97_14792-96insCAGT
NM_206933.3:c.14792-97_14792-96insCAGT	NP_996816.2:n.14792-97_14792-96insCAGT
NM_206933.4:c.14792-97_14792-96insCAGT MANE Select	NP_996816.3:n.14792-97_14792-96insCAGT