Canonical Allele Identifier: CA2747729441
Gene: USH2A HGNC NCBI

Genomic Alleles

HGVS Genome Assembly
NC_000001.11:g.216070449_216070450insACAG , CM000663.2:g.216070449_216070450insACAG GRCh38
NC_000001.10:g.216243791_216243792insACAG , CM000663.1:g.216243791_216243792insACAG GRCh37
NC_000001.9:g.214310414_214310415insACAG NCBI36
NG_009497.1:g.357947_357948insCTGT
NG_009497.2:g.357999_358000insCTGT

Transcript Alleles

HGVS Amino-acid Change
ENST00000307340.8:c.5858-158_5858-157insCTGT MANE Select ENSP00000305941.3:n.5858-158_5858-157insCTGT
ENST00000674083.1:c.5858-158_5858-157insCTGT ENSP00000501296.1:n.5858-158_5858-157insCTGT
ENST00000307340.7:c.5858-158_5858-157insCTGT ENSP00000305941.3:n.5858-158_5858-157insCTGT
NM_206933.2:c.5858-158_5858-157insCTGT NP_996816.2:n.5858-158_5858-157insCTGT
NM_206933.3:c.5858-158_5858-157insCTGT NP_996816.2:n.5858-158_5858-157insCTGT
NM_206933.4:c.5858-158_5858-157insCTGT MANE Select NP_996816.3:n.5858-158_5858-157insCTGT