Canonical Allele Identifier: CA1220374001
Gene: USH2A HGNC NCBI

Genomic Alleles

HGVS Genome Assembly
NC_000001.11:g.215675614T= , CM000663.2:g.215675614T= GRCh38
NC_000001.10:g.215848956T= , CM000663.1:g.215848956T= GRCh37
NC_000001.9:g.213915579T= NCBI36
NG_009497.1:g.752783A=
NG_009497.2:g.752835A=

Transcript Alleles

HGVS Amino-acid Change
ENST00000307340.8:c.12297A= MANE Select ENSP00000305941.3:p.Thr4099=
ENST00000674083.1:c.12297A= ENSP00000501296.1:p.Thr4099=
ENST00000307340.7:c.12297A= ENSP00000305941.3:p.Thr4099=
NM_206933.2:c.12297A= NP_996816.2:p.Thr4099=
NM_206933.3:c.12297A= NP_996816.2:p.Thr4099=
NM_206933.4:c.12297A= MANE Select NP_996816.3:p.Thr4099=