Canonical Allele Identifier: CA423430940

Gene: USH2A USH2A-AS1

Linked Data

• gnomAD v4: 1-216198337-G-C
• MyVariant Identifiers: chr1:g.216371679G>C (hg19)

Genomic Alleles

HGVS	Genome Assembly
NC_000001.11:g.216198337G>C , CM000663.2:g.216198337G>C	GRCh38
NC_000001.10:g.216371679G>C , CM000663.1:g.216371679G>C	GRCh37
NC_000001.9:g.214438302G>C	NCBI36
NG_009497.1:g.230060C>G
NG_009497.2:g.230112C>G

Transcript Alleles

HGVS	Amino-acid Change
ENST00000307340.8:c.4059C>G (USH2A) MANE Select	ENSP00000305941.3:p.Val1353=
ENST00000674083.1:c.4059C>G (USH2A)	ENSP00000501296.1:p.Val1353=
ENST00000307340.7:c.4059C>G (USH2A)	ENSP00000305941.3:p.Val1353=
ENST00000366942.3:c.4059C>G (USH2A)	ENSP00000355909.3:p.Val1353=
NM_007123.5:c.4059C>G (USH2A)	NP_009054.5:p.Val1353=
NM_206933.2:c.4059C>G (USH2A)	NP_996816.2:p.Val1353=
XR_922595.1:n.354+2412G>C (USH2A-AS1)
XR_922596.1:n.354+2412G>C (USH2A-AS1)
XR_922597.1:n.354+2412G>C (USH2A-AS1)
XR_922598.1:n.484+2412G>C (USH2A-AS1)
XR_922595.3:n.1076+2412G>C (USH2A-AS1)
XR_922596.3:n.1076+2412G>C (USH2A-AS1)
NM_206933.3:c.4059C>G (USH2A)	NP_996816.2:p.Val1353=
NM_007123.6:c.4059C>G (USH2A)	NP_009054.6:p.Val1353=
NM_206933.4:c.4059C>G (USH2A) MANE Select	NP_996816.3:p.Val1353=