Canonical Allele Identifier: CA2747719148
Gene: USH2A HGNC NCBI

Genomic Alleles

HGVS Genome Assembly
NC_000001.11:g.215728505_215728506insAC , CM000663.2:g.215728505_215728506insAC GRCh38
NC_000001.10:g.215901847_215901848insAC , CM000663.1:g.215901847_215901848insAC GRCh37
NC_000001.9:g.213968470_213968471insAC NCBI36
NG_009497.1:g.699892_699893insTG
NG_009497.2:g.699944_699945insTG

Transcript Alleles

HGVS Amino-acid Change
ENST00000307340.8:c.11712-121_11712-120insTG MANE Select ENSP00000305941.3:n.11712-121_11712-120insTG
ENST00000674083.1:c.11712-121_11712-120insTG ENSP00000501296.1:n.11712-121_11712-120insTG
ENST00000307340.7:c.11712-121_11712-120insTG ENSP00000305941.3:n.11712-121_11712-120insTG
NM_206933.2:c.11712-121_11712-120insTG NP_996816.2:n.11712-121_11712-120insTG
NM_206933.3:c.11712-121_11712-120insTG NP_996816.2:n.11712-121_11712-120insTG
NM_206933.4:c.11712-121_11712-120insTG MANE Select NP_996816.3:n.11712-121_11712-120insTG