Canonical Allele Identifier: CA1220598761
Gene: USH2A HGNC NCBI
USH2A-AS1 HGNC NCBI

Genomic Alleles

HGVS Genome Assembly
NC_000001.11:g.216200056_216200057delinsTG , CM000663.2:g.216200056_216200057delinsTG GRCh38
NC_000001.10:g.216373398_216373399delinsTG , CM000663.1:g.216373398_216373399delinsTG GRCh37
NC_000001.9:g.214440021_214440022delinsTG NCBI36
NG_009497.1:g.228340_228341delinsCA
NG_009497.2:g.228392_228393delinsCA

Transcript Alleles

HGVS Amino-acid Change
ENST00000307340.8:c.3381_3382delinsCA (USH2A) MANE Select ENSP00000305941.3:p.Thr1127=
ENST00000674083.1:c.3381_3382delinsCA (USH2A) ENSP00000501296.1:p.Thr1127=
ENST00000307340.7:c.3381_3382delinsCA (USH2A) ENSP00000305941.3:p.Thr1127=
ENST00000366942.3:c.3381_3382delinsCA (USH2A) ENSP00000355909.3:p.Thr1127=
NM_007123.5:c.3381_3382delinsCA (USH2A) NP_009054.5:p.Thr1127=
NM_206933.2:c.3381_3382delinsCA (USH2A) NP_996816.2:p.Thr1127=
XR_922595.1:n.355-3974_355-3973delinsTG (USH2A-AS1)
XR_922596.1:n.354+4131_354+4132delinsTG (USH2A-AS1)
XR_922597.1:n.354+4131_354+4132delinsTG (USH2A-AS1)
XR_922598.1:n.485-3974_485-3973delinsTG (USH2A-AS1)
XR_922595.3:n.1077-3974_1077-3973delinsTG (USH2A-AS1)
XR_922596.3:n.1076+4131_1076+4132delinsTG (USH2A-AS1)
NM_206933.3:c.3381_3382delinsCA (USH2A) NP_996816.2:p.Thr1127=
NM_007123.6:c.3381_3382delinsCA (USH2A) NP_009054.6:p.Thr1127=
NM_206933.4:c.3381_3382delinsCA (USH2A) MANE Select NP_996816.3:p.Thr1127=