Canonical Allele Identifier: CA1220652928
Gene: USH2A HGNC NCBI

Genomic Alleles

HGVS Genome Assembly
NC_000001.11:g.216325403_216325406delinsCATT , CM000663.2:g.216325403_216325406delinsCATT GRCh38
NC_000001.10:g.216498745_216498748delinsCATT , CM000663.1:g.216498745_216498748delinsCATT GRCh37
NC_000001.9:g.214565368_214565371delinsCATT NCBI36
NG_009497.1:g.102991_102994delinsAATG
NG_009497.2:g.103043_103046delinsAATG

Transcript Alleles

HGVS Amino-acid Change
ENST00000307340.8:c.1042_1045delinsAATG MANE Select ENSP00000305941.3:p.Asn348=
ENST00000674083.1:c.1042_1045delinsAATG ENSP00000501296.1:p.Asn348=
ENST00000307340.7:c.1042_1045delinsAATG ENSP00000305941.3:p.Asn348=
ENST00000366942.3:c.1042_1045delinsAATG ENSP00000355909.3:p.Asn348=
NM_007123.5:c.1042_1045delinsAATG NP_009054.5:p.Asn348=
NM_206933.2:c.1042_1045delinsAATG NP_996816.2:p.Asn348=
NM_206933.3:c.1042_1045delinsAATG NP_996816.2:p.Asn348=
NM_007123.6:c.1042_1045delinsAATG NP_009054.6:p.Asn348=
NM_206933.4:c.1042_1045delinsAATG MANE Select NP_996816.3:p.Asn348=