Canonical Allele Identifier: CA1012179388
Gene: USH2A HGNC NCBI

Linked Data

dbSNP Id: rs1658001112

Genomic Alleles

HGVS Genome Assembly
NC_000001.11:g.215675697_215675699del , CM000663.2:g.215675697_215675699del GRCh38
NC_000001.10:g.215849039_215849041del , CM000663.1:g.215849039_215849041del GRCh37
NC_000001.9:g.213915662_213915664del NCBI36
NG_009497.1:g.752699_752701del
NG_009497.2:g.752751_752753del

Transcript Alleles

HGVS Amino-acid Change
ENST00000307340.8:c.12295-82_12295-80del MANE Select ENSP00000305941.3:n.12295-82_12295-80del
ENST00000674083.1:c.12295-82_12295-80del ENSP00000501296.1:n.12295-82_12295-80del
ENST00000307340.7:c.12295-82_12295-80del ENSP00000305941.3:n.12295-82_12295-80del
NM_206933.2:c.12295-82_12295-80del NP_996816.2:n.12295-82_12295-80del
NM_206933.3:c.12295-82_12295-80del NP_996816.2:n.12295-82_12295-80del
NM_206933.4:c.12295-82_12295-80del MANE Select NP_996816.3:n.12295-82_12295-80del