Canonical Allele Identifier: CA1142238652

Gene: USH2A

Genomic Alleles

HGVS	Genome Assembly
NC_000001.11:g.215780241A= , CM000663.2:g.215780241A=	GRCh38
NC_000001.10:g.215953583A= , CM000663.1:g.215953583A=	GRCh37
NC_000001.9:g.214020206A=	NCBI36
NG_009497.1:g.648156T=
NG_009497.2:g.648208T=

Transcript Alleles

HGVS	Amino-acid Change
ENST00000307340.8:c.10741-200T= MANE Select	ENSP00000305941.3:n.10741-200T=
ENST00000674083.1:c.10741-200T=	ENSP00000501296.1:n.10741-200T=
ENST00000307340.7:c.10741-200T=	ENSP00000305941.3:n.10741-200T=
NM_206933.2:c.10741-200T=	NP_996816.2:n.10741-200T=
NM_206933.3:c.10741-200T=	NP_996816.2:n.10741-200T=
NM_206933.4:c.10741-200T= MANE Select	NP_996816.3:n.10741-200T=