Canonical Allele Identifier: CA423396259

Gene: USH2A

Linked Data

• MyVariant Identifiers: chr1:g.216591937T>A (hg19)

Genomic Alleles

HGVS	Genome Assembly
NC_000001.11:g.216418595T>A , CM000663.2:g.216418595T>A	GRCh38
NC_000001.10:g.216591937T>A , CM000663.1:g.216591937T>A	GRCh37
NC_000001.9:g.214658560T>A	NCBI36
NG_009497.1:g.9802A>T
NG_009497.2:g.9854A>T

Transcript Alleles

HGVS	Amino-acid Change
ENST00000307340.8:c.570A>T MANE Select	ENSP00000305941.3:p.Thr190=
ENST00000674083.1:c.570A>T	ENSP00000501296.1:p.Thr190=
ENST00000307340.7:c.570A>T	ENSP00000305941.3:p.Thr190=
ENST00000366942.3:c.570A>T	ENSP00000355909.3:p.Thr190=
NM_007123.5:c.570A>T	NP_009054.5:p.Thr190=
NM_206933.2:c.570A>T	NP_996816.2:p.Thr190=
NM_206933.3:c.570A>T	NP_996816.2:p.Thr190=
NM_007123.6:c.570A>T	NP_009054.6:p.Thr190=
NM_206933.4:c.570A>T MANE Select	NP_996816.3:p.Thr190=