Canonical Allele Identifier: CA1220416786

Gene: USH2A

Genomic Alleles

HGVS	Genome Assembly
NC_000001.11:g.215782195A= , CM000663.2:g.215782195A=	GRCh38
NC_000001.10:g.215955537A= , CM000663.1:g.215955537A=	GRCh37
NC_000001.9:g.214022160A=	NCBI36
NG_009497.1:g.646202T=
NG_009497.2:g.646254T=

Transcript Alleles

HGVS	Amino-acid change
ENST00000307340.8:c.10587T= MANE Select	ENSP00000305941.3:p.Gly3529=
ENST00000674083.1:c.10587T=	ENSP00000501296.1:p.Gly3529=
ENST00000307340.7:c.10587T=	ENSP00000305941.3:p.Gly3529=
NM_206933.2:c.10587T=	NP_996816.2:p.Gly3529=
NM_206933.3:c.10587T=	NP_996816.2:p.Gly3529=
NM_206933.4:c.10587T= MANE Select	NP_996816.3:p.Gly3529=