Canonical Allele Identifier: CA2747721919

Gene: USH2A

Genomic Alleles

HGVS	Genome Assembly
NC_000001.11:g.215799212_215799214del , CM000663.2:g.215799212_215799214del	GRCh38
NC_000001.10:g.215972554_215972556del , CM000663.1:g.215972554_215972556del	GRCh37
NC_000001.9:g.214039177_214039179del	NCBI36
NG_009497.1:g.629183_629185del
NG_009497.2:g.629235_629237del

Transcript Alleles

HGVS	Amino-acid Change
ENST00000307340.8:c.9740-89_9740-87del MANE Select	ENSP00000305941.3:n.9740-89_9740-87del
ENST00000674083.1:c.9740-89_9740-87del	ENSP00000501296.1:n.9740-89_9740-87del
ENST00000307340.7:c.9740-89_9740-87del	ENSP00000305941.3:n.9740-89_9740-87del
NM_206933.2:c.9740-89_9740-87del	NP_996816.2:n.9740-89_9740-87del
NM_206933.3:c.9740-89_9740-87del	NP_996816.2:n.9740-89_9740-87del
NM_206933.4:c.9740-89_9740-87del MANE Select	NP_996816.3:n.9740-89_9740-87del