Canonical Allele Identifier: CA1220455831
Gene: USH2A HGNC NCBI

Genomic Alleles

HGVS Genome Assembly
NC_000001.11:g.215867429T= , CM000663.2:g.215867429T= GRCh38
NC_000001.10:g.216040771T= , CM000663.1:g.216040771T= GRCh37
NC_000001.9:g.214107394T= NCBI36
NG_009497.1:g.560968A=
NG_009497.2:g.561020A=

Transcript Alleles

HGVS Amino-acid Change
ENST00000307340.8:c.8682-259A= MANE Select ENSP00000305941.3:n.8682-259A=
ENST00000674083.1:c.8682-259A= ENSP00000501296.1:n.8682-259A=
ENST00000307340.7:c.8682-259A= ENSP00000305941.3:n.8682-259A=
NM_206933.2:c.8682-259A= NP_996816.2:n.8682-259A=
NM_206933.3:c.8682-259A= NP_996816.2:n.8682-259A=
NM_206933.4:c.8682-259A= MANE Select NP_996816.3:n.8682-259A=