Canonical Allele Identifier: CA1220373837
Gene: USH2A HGNC NCBI

Genomic Alleles

HGVS Genome Assembly
NC_000001.11:g.215675167_215675172delinsATGCCC , CM000663.2:g.215675167_215675172delinsATGCCC GRCh38
NC_000001.10:g.215848509_215848514delinsATGCCC , CM000663.1:g.215848509_215848514delinsATGCCC GRCh37
NC_000001.9:g.213915132_213915137delinsATGCCC NCBI36
NG_009497.1:g.753225_753230delinsGGGCAT
NG_009497.2:g.753277_753282delinsGGGCAT

Transcript Alleles

HGVS Amino-acid Change
ENST00000307340.8:c.12739_12744delinsGGGCAT MANE Select ENSP00000305941.3:p.Gly4247=
ENST00000674083.1:c.12739_12744delinsGGGCAT ENSP00000501296.1:p.Gly4247=
ENST00000307340.7:c.12739_12744delinsGGGCAT ENSP00000305941.3:p.Gly4247=
NM_206933.2:c.12739_12744delinsGGGCAT NP_996816.2:p.Gly4247=
NM_206933.3:c.12739_12744delinsGGGCAT NP_996816.2:p.Gly4247=
NM_206933.4:c.12739_12744delinsGGGCAT MANE Select NP_996816.3:p.Gly4247=