Canonical Allele Identifier: CA1220412650
Gene: USH2A HGNC NCBI

Genomic Alleles

HGVS Genome Assembly
NC_000001.11:g.215766665G= , CM000663.2:g.215766665G= GRCh38
NC_000001.10:g.215940007G= , CM000663.1:g.215940007G= GRCh37
NC_000001.9:g.214006630G= NCBI36
NG_009497.1:g.661732C=
NG_009497.2:g.661784C=

Transcript Alleles

HGVS Amino-acid change
ENST00000307340.8:c.11047+16C= MANE Select ENSP00000305941.3:n.11047+16C=
ENST00000674083.1:c.11047+16C= ENSP00000501296.1:n.11047+16C=
ENST00000307340.7:c.11047+16C= ENSP00000305941.3:n.11047+16C=
NM_206933.2:c.11047+16C= NP_996816.2:n.11047+16C=
NM_206933.3:c.11047+16C= NP_996816.2:n.11047+16C=
NM_206933.4:c.11047+16C= MANE Select NP_996816.3:n.11047+16C=