Canonical Allele Identifier: CA344902481

Gene: USH2A

Linked Data

• MyVariant Identifiers: chr1:g.216591929C>G (hg19) ; chr1:g.216418587C>G (hg38)

Genomic Alleles

HGVS	Genome Assembly
NC_000001.11:g.216418587C>G , CM000663.2:g.216418587C>G	GRCh38
NC_000001.10:g.216591929C>G , CM000663.1:g.216591929C>G	GRCh37
NC_000001.9:g.214658552C>G	NCBI36
NG_009497.1:g.9810G>C
NG_009497.2:g.9862G>C

Transcript Alleles

HGVS	Amino-acid Change
ENST00000307340.8:c.578G>C MANE Select	ENSP00000305941.3:p.Gly193Ala
ENST00000674083.1:c.578G>C	ENSP00000501296.1:p.Gly193Ala
ENST00000307340.7:c.578G>C	ENSP00000305941.3:p.Gly193Ala
ENST00000366942.3:c.578G>C	ENSP00000355909.3:p.Gly193Ala
NM_007123.5:c.578G>C	NP_009054.5:p.Gly193Ala
NM_206933.2:c.578G>C	NP_996816.2:p.Gly193Ala
NM_206933.3:c.578G>C	NP_996816.2:p.Gly193Ala
NM_007123.6:c.578G>C	NP_009054.6:p.Gly193Ala
NM_206933.4:c.578G>C MANE Select	NP_996816.3:p.Gly193Ala