Canonical Allele Identifier: CA1143363434
Gene: USH2A HGNC NCBI

Genomic Alleles

HGVS Genome Assembly
NC_000001.11:g.215675336C= , CM000663.2:g.215675336C= GRCh38
NC_000001.10:g.215848678C= , CM000663.1:g.215848678C= GRCh37
NC_000001.9:g.213915301C= NCBI36
NG_009497.1:g.753061G=
NG_009497.2:g.753113G=

Transcript Alleles

HGVS Amino-acid Change
ENST00000307340.8:c.12575G= MANE Select ENSP00000305941.3:p.Arg4192=
ENST00000674083.1:c.12575G= ENSP00000501296.1:p.Arg4192=
ENST00000307340.7:c.12575G= ENSP00000305941.3:p.Arg4192=
NM_206933.2:c.12575G= NP_996816.2:p.Arg4192=
NM_206933.3:c.12575G= NP_996816.2:p.Arg4192=
NM_206933.4:c.12575G= MANE Select NP_996816.3:p.Arg4192=