Canonical Allele Identifier: CA1220363137
Community Standard Title: NM_206933.4(USH2A):c.14582+7G=
Gene: USH2A HGNC NCBI

Genomic Alleles

HGVS Genome Assembly
NC_000001.11:g.215648521C= , CM000663.2:g.215648521C= GRCh38
NC_000001.10:g.215821863C= , CM000663.1:g.215821863C= GRCh37
NC_000001.9:g.213888486C= NCBI36
NG_009497.1:g.779876G=
NG_009497.2:g.779928G=

Transcript Alleles

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