Canonical Allele Identifier: CA1220461538

Gene: USH2A

Genomic Alleles

HGVS	Genome Assembly
NC_000001.11:g.215878800C= , CM000663.2:g.215878800C=	GRCh38
NC_000001.10:g.216052142C= , CM000663.1:g.216052142C=	GRCh37
NC_000001.9:g.214118765C=	NCBI36
NG_009497.1:g.549597G=
NG_009497.2:g.549649G=

Transcript Alleles

HGVS	Amino-acid Change
ENST00000307340.8:c.8522G= MANE Select	ENSP00000305941.3:p.Trp2841=
ENST00000674083.1:c.8522G=	ENSP00000501296.1:p.Trp2841=
ENST00000307340.7:c.8522G=	ENSP00000305941.3:p.Trp2841=
NM_206933.2:c.8522G=	NP_996816.2:p.Trp2841=
NM_206933.3:c.8522G=	NP_996816.2:p.Trp2841=
NM_206933.4:c.8522G= MANE Select	NP_996816.3:p.Trp2841=