Canonical Allele Identifier: CA1220396479
Gene: USH2A HGNC NCBI

Genomic Alleles

HGVS Genome Assembly
NC_000001.11:g.215728067G= , CM000663.2:g.215728067G= GRCh38
NC_000001.10:g.215901409G= , CM000663.1:g.215901409G= GRCh37
NC_000001.9:g.213968032G= NCBI36
NG_009497.1:g.700330C=
NG_009497.2:g.700382C=

Transcript Alleles

HGVS Amino-acid Change
ENST00000307340.8:c.12029C= MANE Select ENSP00000305941.3:p.Thr4010=
ENST00000674083.1:c.12029C= ENSP00000501296.1:p.Thr4010=
ENST00000307340.7:c.12029C= ENSP00000305941.3:p.Thr4010=
NM_206933.2:c.12029C= NP_996816.2:p.Thr4010=
NM_206933.3:c.12029C= NP_996816.2:p.Thr4010=
NM_206933.4:c.12029C= MANE Select NP_996816.3:p.Thr4010=