Canonical Allele Identifier: CA2747729435
Gene: USH2A HGNC NCBI

Genomic Alleles

HGVS Genome Assembly
NC_000001.11:g.216070433_216070435del , CM000663.2:g.216070433_216070435del GRCh38
NC_000001.10:g.216243775_216243777del , CM000663.1:g.216243775_216243777del GRCh37
NC_000001.9:g.214310398_214310400del NCBI36
NG_009497.1:g.357962_357964del
NG_009497.2:g.358014_358016del

Transcript Alleles

HGVS Amino-acid Change
ENST00000307340.8:c.5858-143_5858-141del MANE Select ENSP00000305941.3:n.5858-143_5858-141del
ENST00000674083.1:c.5858-143_5858-141del ENSP00000501296.1:n.5858-143_5858-141del
ENST00000307340.7:c.5858-143_5858-141del ENSP00000305941.3:n.5858-143_5858-141del
NM_206933.2:c.5858-143_5858-141del NP_996816.2:n.5858-143_5858-141del
NM_206933.3:c.5858-143_5858-141del NP_996816.2:n.5858-143_5858-141del
NM_206933.4:c.5858-143_5858-141del MANE Select NP_996816.3:n.5858-143_5858-141del