Canonical Allele Identifier: CA1144233401

Gene: USH2A

Genomic Alleles

HGVS	Genome Assembly
NC_000001.11:g.215674445C= , CM000663.2:g.215674445C=	GRCh38
NC_000001.10:g.215847787C= , CM000663.1:g.215847787C=	GRCh37
NC_000001.9:g.213914410C=	NCBI36
NG_009497.1:g.753952G=
NG_009497.2:g.754004G=

Transcript Alleles

HGVS	Amino-acid Change
ENST00000307340.8:c.13466G= MANE Select	ENSP00000305941.3:p.Gly4489=
ENST00000674083.1:c.13466G=	ENSP00000501296.1:p.Gly4489=
ENST00000307340.7:c.13466G=	ENSP00000305941.3:p.Gly4489=
NM_206933.2:c.13466G=	NP_996816.2:p.Gly4489=
NM_206933.3:c.13466G=	NP_996816.2:p.Gly4489=
NM_206933.4:c.13466G= MANE Select	NP_996816.3:p.Gly4489=