Canonical Allele Identifier: CA2747734198
Gene: USH2A HGNC NCBI
USH2A-AS1 HGNC NCBI

Genomic Alleles

HGVS Genome Assembly
NC_000001.11:g.216198306G>T , CM000663.2:g.216198306G>T GRCh38
NC_000001.10:g.216371648G>T , CM000663.1:g.216371648G>T GRCh37
NC_000001.9:g.214438271G>T NCBI36
NG_009497.1:g.230091C>A
NG_009497.2:g.230143C>A

Transcript Alleles

HGVS Amino-acid Change
ENST00000307340.8:c.4081+9C>A (USH2A) MANE Select ENSP00000305941.3:n.4081+9C>A
ENST00000674083.1:c.4081+9C>A (USH2A) ENSP00000501296.1:n.4081+9C>A
ENST00000307340.7:c.4081+9C>A (USH2A) ENSP00000305941.3:n.4081+9C>A
ENST00000366942.3:c.4081+9C>A (USH2A) ENSP00000355909.3:n.4081+9C>A
NM_007123.5:c.4081+9C>A (USH2A) NP_009054.5:n.4081+9C>A
NM_206933.2:c.4081+9C>A (USH2A) NP_996816.2:n.4081+9C>A
XR_922595.1:n.354+2381G>T (USH2A-AS1)
XR_922596.1:n.354+2381G>T (USH2A-AS1)
XR_922597.1:n.354+2381G>T (USH2A-AS1)
XR_922598.1:n.484+2381G>T (USH2A-AS1)
XR_922595.3:n.1076+2381G>T (USH2A-AS1)
XR_922596.3:n.1076+2381G>T (USH2A-AS1)
NM_206933.3:c.4081+9C>A (USH2A) NP_996816.2:n.4081+9C>A
NM_007123.6:c.4081+9C>A (USH2A) NP_009054.6:n.4081+9C>A
NM_206933.4:c.4081+9C>A (USH2A) MANE Select NP_996816.3:n.4081+9C>A