Canonical Allele Identifier: CA1144115369
Gene: USH2A HGNC NCBI

Genomic Alleles

HGVS Genome Assembly
NC_000001.11:g.215675609T= , CM000663.2:g.215675609T= GRCh38
NC_000001.10:g.215848951T= , CM000663.1:g.215848951T= GRCh37
NC_000001.9:g.213915574T= NCBI36
NG_009497.1:g.752788A=
NG_009497.2:g.752840A=

Transcript Alleles

HGVS Amino-acid Change
ENST00000307340.8:c.12302A= MANE Select ENSP00000305941.3:p.Asn4101=
ENST00000674083.1:c.12302A= ENSP00000501296.1:p.Asn4101=
ENST00000307340.7:c.12302A= ENSP00000305941.3:p.Asn4101=
NM_206933.2:c.12302A= NP_996816.2:p.Asn4101=
NM_206933.3:c.12302A= NP_996816.2:p.Asn4101=
NM_206933.4:c.12302A= MANE Select NP_996816.3:p.Asn4101=