Canonical Allele Identifier: CA2650500250
Community Standard Title: NM_206933.4(USH2A):c.14582+13G>A
Gene: USH2A HGNC NCBI

Genomic Alleles

HGVS Genome Assembly
NC_000001.11:g.215648515C>T , CM000663.2:g.215648515C>T GRCh38
NC_000001.10:g.215821857C>T , CM000663.1:g.215821857C>T GRCh37
NC_000001.9:g.213888480C>T NCBI36
NG_009497.1:g.779882G>A
NG_009497.2:g.779934G>A

Transcript Alleles

HGVS Amino-acid Change
NM_206933.4:c.14582+13G>A MANE Select NP_996816.3:n.14582+13G>A
ENST00000307340.8:c.14582+13G>A MANE Select ENSP00000305941.3:n.14582+13G>A
NM_206933.2:c.14582+13G>A NP_996816.2:n.14582+13G>A
NM_206933.3:c.14582+13G>A NP_996816.2:n.14582+13G>A
ENST00000307340.7:c.14582+13G>A ENSP00000305941.3:n.14582+13G>A
ENST00000674083.1:c.14582+13G>A ENSP00000501296.1:n.14582+13G>A