Canonical Allele Identifier: CA2747719134
Gene: USH2A HGNC NCBI

Genomic Alleles

HGVS Genome Assembly
NC_000001.11:g.215728486_215728487insAGT , CM000663.2:g.215728486_215728487insAGT GRCh38
NC_000001.10:g.215901828_215901829insAGT , CM000663.1:g.215901828_215901829insAGT GRCh37
NC_000001.9:g.213968451_213968452insAGT NCBI36
NG_009497.1:g.699910_699911insACT
NG_009497.2:g.699962_699963insACT

Transcript Alleles

HGVS Amino-acid Change
ENST00000307340.8:c.11712-103_11712-102insACT MANE Select ENSP00000305941.3:n.11712-103_11712-102insACT
ENST00000674083.1:c.11712-103_11712-102insACT ENSP00000501296.1:n.11712-103_11712-102insACT
ENST00000307340.7:c.11712-103_11712-102insACT ENSP00000305941.3:n.11712-103_11712-102insACT
NM_206933.2:c.11712-103_11712-102insACT NP_996816.2:n.11712-103_11712-102insACT
NM_206933.3:c.11712-103_11712-102insACT NP_996816.2:n.11712-103_11712-102insACT
NM_206933.4:c.11712-103_11712-102insACT MANE Select NP_996816.3:n.11712-103_11712-102insACT