Canonical Allele Identifier: CA344833834
Community Standard Title: NM_206933.4(USH2A):c.14429G>C (p.Cys4810Ser)
Gene: USH2A HGNC NCBI

Genomic Alleles

HGVS Genome Assembly
NC_000001.11:g.215648681C>G , CM000663.2:g.215648681C>G GRCh38
NC_000001.10:g.215822023C>G , CM000663.1:g.215822023C>G GRCh37
NC_000001.9:g.213888646C>G NCBI36
NG_009497.1:g.779716G>C
NG_009497.2:g.779768G>C

Transcript Alleles

HGVS Amino-acid Change
NM_206933.4:c.14429G>C MANE Select NP_996816.3:p.Cys4810Ser
ENST00000307340.8:c.14429G>C MANE Select ENSP00000305941.3:p.Cys4810Ser
NM_206933.2:c.14429G>C NP_996816.2:p.Cys4810Ser
NM_206933.3:c.14429G>C NP_996816.2:p.Cys4810Ser
ENST00000307340.7:c.14429G>C ENSP00000305941.3:p.Cys4810Ser
ENST00000674083.1:c.14429G>C ENSP00000501296.1:p.Cys4810Ser