Canonical Allele Identifier: CA3077339317
Community Standard Title: NM_206933.4(USH2A):c.14389G= (p.Ala4797=)
Gene: USH2A HGNC NCBI

Genomic Alleles

HGVS Genome Assembly
NC_000001.11:g.215648721C= , CM000663.2:g.215648721C= GRCh38
NC_000001.10:g.215822063C= , CM000663.1:g.215822063C= GRCh37
NC_000001.9:g.213888686C= NCBI36
NG_009497.1:g.779676G=
NG_009497.2:g.779728G=

Transcript Alleles

HGVS Amino-acid Change
NM_206933.4:c.14389G= MANE Select NP_996816.3:p.Ala4797=
ENST00000307340.8:c.14389G= MANE Select ENSP00000305941.3:p.Ala4797=
NM_206933.2:c.14389G= NP_996816.2:p.Ala4797=
NM_206933.3:c.14389G= NP_996816.2:p.Ala4797=
ENST00000307340.7:c.14389G= ENSP00000305941.3:p.Ala4797=
ENST00000674083.1:c.14389G= ENSP00000501296.1:p.Ala4797=