Canonical Allele Identifier: CA2747721953
Gene: USH2A HGNC NCBI

Genomic Alleles

HGVS Genome Assembly
NC_000001.11:g.215799291_215799296del , CM000663.2:g.215799291_215799296del GRCh38
NC_000001.10:g.215972633_215972638del , CM000663.1:g.215972633_215972638del GRCh37
NC_000001.9:g.214039256_214039261del NCBI36
NG_009497.1:g.629103_629108del
NG_009497.2:g.629155_629160del

Transcript Alleles

HGVS Amino-acid Change
ENST00000307340.8:c.9740-169_9740-164del MANE Select ENSP00000305941.3:n.9740-169_9740-164del
ENST00000674083.1:c.9740-169_9740-164del ENSP00000501296.1:n.9740-169_9740-164del
ENST00000307340.7:c.9740-169_9740-164del ENSP00000305941.3:n.9740-169_9740-164del
NM_206933.2:c.9740-169_9740-164del NP_996816.2:n.9740-169_9740-164del
NM_206933.3:c.9740-169_9740-164del NP_996816.2:n.9740-169_9740-164del
NM_206933.4:c.9740-169_9740-164del MANE Select NP_996816.3:n.9740-169_9740-164del