Canonical Allele Identifier: CA529001989
Community Standard Title: NM_206933.4(USH2A):c.14582+21A>T
Gene: USH2A HGNC NCBI

Genomic Alleles

HGVS Genome Assembly
NC_000001.11:g.215648507T>A , CM000663.2:g.215648507T>A GRCh38
NC_000001.10:g.215821849T>A , CM000663.1:g.215821849T>A GRCh37
NC_000001.9:g.213888472T>A NCBI36
NG_009497.1:g.779890A>T
NG_009497.2:g.779942A>T

Transcript Alleles

HGVS Amino-acid Change
NM_206933.4:c.14582+21A>T MANE Select NP_996816.3:n.14582+21A>T
ENST00000307340.8:c.14582+21A>T MANE Select ENSP00000305941.3:n.14582+21A>T
NM_206933.2:c.14582+21A>T NP_996816.2:n.14582+21A>T
NM_206933.3:c.14582+21A>T NP_996816.2:n.14582+21A>T
ENST00000307340.7:c.14582+21A>T ENSP00000305941.3:n.14582+21A>T
ENST00000674083.1:c.14582+21A>T ENSP00000501296.1:n.14582+21A>T