Canonical Allele Identifier: CA2747720434
Gene: USH2A HGNC NCBI

Genomic Alleles

HGVS Genome Assembly
NC_000001.11:g.215766954_215766958del , CM000663.2:g.215766954_215766958del GRCh38
NC_000001.10:g.215940296_215940300del , CM000663.1:g.215940296_215940300del GRCh37
NC_000001.9:g.214006919_214006923del NCBI36
NG_009497.1:g.661439_661443del
NG_009497.2:g.661491_661495del

Transcript Alleles

HGVS Amino-acid Change
ENST00000307340.8:c.10940-170_10940-166del MANE Select ENSP00000305941.3:n.10940-170_10940-166del
ENST00000674083.1:c.10940-170_10940-166del ENSP00000501296.1:n.10940-170_10940-166del
ENST00000307340.7:c.10940-170_10940-166del ENSP00000305941.3:n.10940-170_10940-166del
NM_206933.2:c.10940-170_10940-166del NP_996816.2:n.10940-170_10940-166del
NM_206933.3:c.10940-170_10940-166del NP_996816.2:n.10940-170_10940-166del
NM_206933.4:c.10940-170_10940-166del MANE Select NP_996816.3:n.10940-170_10940-166del