Canonical Allele Identifier: CA2747721886

Gene: USH2A

Genomic Alleles

HGVS	Genome Assembly
NC_000001.11:g.215799178_215799182del , CM000663.2:g.215799178_215799182del	GRCh38
NC_000001.10:g.215972520_215972524del , CM000663.1:g.215972520_215972524del	GRCh37
NC_000001.9:g.214039143_214039147del	NCBI36
NG_009497.1:g.629215_629219del
NG_009497.2:g.629267_629271del

Transcript Alleles

HGVS	Amino-acid Change
ENST00000307340.8:c.9740-57_9740-53del MANE Select	ENSP00000305941.3:n.9740-57_9740-53del
ENST00000674083.1:c.9740-57_9740-53del	ENSP00000501296.1:n.9740-57_9740-53del
ENST00000307340.7:c.9740-57_9740-53del	ENSP00000305941.3:n.9740-57_9740-53del
NM_206933.2:c.9740-57_9740-53del	NP_996816.2:n.9740-57_9740-53del
NM_206933.3:c.9740-57_9740-53del	NP_996816.2:n.9740-57_9740-53del
NM_206933.4:c.9740-57_9740-53del MANE Select	NP_996816.3:n.9740-57_9740-53del