Canonical Allele Identifier: CA2747717688
Gene: USH2A HGNC NCBI

Genomic Alleles

HGVS Genome Assembly
NC_000001.11:g.215675640_215675641insAC , CM000663.2:g.215675640_215675641insAC GRCh38
NC_000001.10:g.215848982_215848983insAC , CM000663.1:g.215848982_215848983insAC GRCh37
NC_000001.9:g.213915605_213915606insAC NCBI36
NG_009497.1:g.752756_752757insGT
NG_009497.2:g.752808_752809insGT

Transcript Alleles

HGVS Amino-acid Change
ENST00000307340.8:c.12295-25_12295-24insGT MANE Select ENSP00000305941.3:n.12295-25_12295-24insGT
ENST00000674083.1:c.12295-25_12295-24insGT ENSP00000501296.1:n.12295-25_12295-24insGT
ENST00000307340.7:c.12295-25_12295-24insGT ENSP00000305941.3:n.12295-25_12295-24insGT
NM_206933.2:c.12295-25_12295-24insGT NP_996816.2:n.12295-25_12295-24insGT
NM_206933.3:c.12295-25_12295-24insGT NP_996816.2:n.12295-25_12295-24insGT
NM_206933.4:c.12295-25_12295-24insGT MANE Select NP_996816.3:n.12295-25_12295-24insGT