Canonical Allele Identifier: CA143494

Gene: USH2A

Linked Data

• ClinVar Variation Id: 48520
• ClinVar RCV Id: RCV000041846 ; RCV000270447 ; RCV000324312 ; RCV000513149 ; RCV001073300
• dbSNP Id: rs41303255
• ExAC: 1:216348635 T / A
• gnomAD v2: 1-216348635-T-A
• gnomAD v3: 1-216175293-T-A
• gnomAD v4: 1-216175293-T-A
• MyVariant Identifiers: chr1:g.216348635T>A (hg19) ; chr1:g.216175293T>A (hg38)

Genomic Alleles

HGVS	Genome Assembly
NC_000001.11:g.216175293T>A , CM000663.2:g.216175293T>A	GRCh38
NC_000001.10:g.216348635T>A , CM000663.1:g.216348635T>A	GRCh37
NC_000001.9:g.214415258T>A	NCBI36
NG_009497.1:g.253104A>T
NG_009497.2:g.253156A>T

Transcript Alleles

HGVS	Amino-acid Change
ENST00000307340.8:c.4586A>T MANE Select	ENSP00000305941.3:p.Lys1529Ile
ENST00000674083.1:c.4586A>T	ENSP00000501296.1:p.Lys1529Ile
ENST00000307340.7:c.4586A>T	ENSP00000305941.3:p.Lys1529Ile
ENST00000366942.3:c.4586A>T	ENSP00000355909.3:p.Lys1529Ile
NM_007123.5:c.4586A>T	NP_009054.5:p.Lys1529Ile
NM_206933.2:c.4586A>T	NP_996816.2:p.Lys1529Ile
NM_206933.3:c.4586A>T	NP_996816.2:p.Lys1529Ile
NM_007123.6:c.4586A>T	NP_009054.6:p.Lys1529Ile
NM_206933.4:c.4586A>T MANE Select	NP_996816.3:p.Lys1529Ile