Canonical Allele Identifier: CA2747717679
Gene: USH2A HGNC NCBI

Genomic Alleles

HGVS Genome Assembly
NC_000001.11:g.215675636_215675638del , CM000663.2:g.215675636_215675638del GRCh38
NC_000001.10:g.215848978_215848980del , CM000663.1:g.215848978_215848980del GRCh37
NC_000001.9:g.213915601_213915603del NCBI36
NG_009497.1:g.752760_752762del
NG_009497.2:g.752812_752814del

Transcript Alleles

HGVS Amino-acid Change
ENST00000307340.8:c.12295-21_12295-19del MANE Select ENSP00000305941.3:n.12295-21_12295-19del
ENST00000674083.1:c.12295-21_12295-19del ENSP00000501296.1:n.12295-21_12295-19del
ENST00000307340.7:c.12295-21_12295-19del ENSP00000305941.3:n.12295-21_12295-19del
NM_206933.2:c.12295-21_12295-19del NP_996816.2:n.12295-21_12295-19del
NM_206933.3:c.12295-21_12295-19del NP_996816.2:n.12295-21_12295-19del
NM_206933.4:c.12295-21_12295-19del MANE Select NP_996816.3:n.12295-21_12295-19del