Canonical Allele Identifier: CA1220652536
Gene: USH2A HGNC NCBI

Genomic Alleles

HGVS Genome Assembly
NC_000001.11:g.216324424T= , CM000663.2:g.216324424T= GRCh38
NC_000001.10:g.216497766T= , CM000663.1:g.216497766T= GRCh37
NC_000001.9:g.214564389T= NCBI36
NG_009497.1:g.103973A=
NG_009497.2:g.104025A=

Transcript Alleles

HGVS Amino-acid Change
ENST00000307340.8:c.1144-72A= MANE Select ENSP00000305941.3:n.1144-72A=
ENST00000674083.1:c.1144-72A= ENSP00000501296.1:n.1144-72A=
ENST00000307340.7:c.1144-72A= ENSP00000305941.3:n.1144-72A=
ENST00000366942.3:c.1144-72A= ENSP00000355909.3:n.1144-72A=
NM_007123.5:c.1144-72A= NP_009054.5:n.1144-72A=
NM_206933.2:c.1144-72A= NP_996816.2:n.1144-72A=
NM_206933.3:c.1144-72A= NP_996816.2:n.1144-72A=
NM_007123.6:c.1144-72A= NP_009054.6:n.1144-72A=
NM_206933.4:c.1144-72A= MANE Select NP_996816.3:n.1144-72A=