Canonical Allele Identifier: CA1142292888
Gene: USH2A HGNC NCBI

Genomic Alleles

HGVS Genome Assembly
NC_000001.11:g.215640633C= , CM000663.2:g.215640633C= GRCh38
NC_000001.10:g.215813975C= , CM000663.1:g.215813975C= GRCh37
NC_000001.9:g.213880598C= NCBI36
NG_009497.1:g.787764G=
NG_009497.2:g.787816G=

Transcript Alleles

HGVS Amino-acid Change
ENST00000307340.8:c.14893G= MANE Select ENSP00000305941.3:p.Val4965=
ENST00000674083.1:c.14893G= ENSP00000501296.1:p.Val4965=
ENST00000307340.7:c.14893G= ENSP00000305941.3:p.Val4965=
NM_206933.2:c.14893G= NP_996816.2:p.Val4965=
NM_206933.3:c.14893G= NP_996816.2:p.Val4965=
NM_206933.4:c.14893G= MANE Select NP_996816.3:p.Val4965=