Canonical Allele Identifier: CA344902513

Gene: USH2A

Linked Data

• MyVariant Identifiers: chr1:g.216591945A>C (hg19) ; chr1:g.216418603A>C (hg38)

Genomic Alleles

HGVS	Genome Assembly
NC_000001.11:g.216418603A>C , CM000663.2:g.216418603A>C	GRCh38
NC_000001.10:g.216591945A>C , CM000663.1:g.216591945A>C	GRCh37
NC_000001.9:g.214658568A>C	NCBI36
NG_009497.1:g.9794T>G
NG_009497.2:g.9846T>G

Transcript Alleles

HGVS	Amino-acid change
ENST00000307340.8:c.562T>G MANE Select	ENSP00000305941.3:p.Tyr188Asp
ENST00000674083.1:c.562T>G	ENSP00000501296.1:p.Tyr188Asp
ENST00000307340.7:c.562T>G	ENSP00000305941.3:p.Tyr188Asp
ENST00000366942.3:c.562T>G	ENSP00000355909.3:p.Tyr188Asp
NM_007123.5:c.562T>G	NP_009054.5:p.Tyr188Asp
NM_206933.2:c.562T>G	NP_996816.2:p.Tyr188Asp
NM_206933.3:c.562T>G	NP_996816.2:p.Tyr188Asp
NM_007123.6:c.562T>G	NP_009054.6:p.Tyr188Asp
NM_206933.4:c.562T>G MANE Select	NP_996816.3:p.Tyr188Asp