Canonical Allele Identifier: CA1220372107
Gene: USH2A HGNC NCBI

Genomic Alleles

HGVS Genome Assembly
NC_000001.11:g.215670948T= , CM000663.2:g.215670948T= GRCh38
NC_000001.10:g.215844290T= , CM000663.1:g.215844290T= GRCh37
NC_000001.9:g.213910913T= NCBI36
NG_009497.1:g.757449A=
NG_009497.2:g.757501A=

Transcript Alleles

HGVS Amino-acid Change
ENST00000307340.8:c.14133+24A= MANE Select ENSP00000305941.3:n.14133+24A=
ENST00000674083.1:c.14133+24A= ENSP00000501296.1:n.14133+24A=
ENST00000307340.7:c.14133+24A= ENSP00000305941.3:n.14133+24A=
NM_206933.2:c.14133+24A= NP_996816.2:n.14133+24A=
NM_206933.3:c.14133+24A= NP_996816.2:n.14133+24A=
NM_206933.4:c.14133+24A= MANE Select NP_996816.3:n.14133+24A=