Canonical Allele Identifier: CA344841190
Gene: USH2A HGNC NCBI

Linked Data

Genomic Alleles

HGVS Genome Assembly
NC_000001.11:g.215671169G>C , CM000663.2:g.215671169G>C GRCh38
NC_000001.10:g.215844511G>C , CM000663.1:g.215844511G>C GRCh37
NC_000001.9:g.213911134G>C NCBI36
NG_009497.1:g.757228C>G
NG_009497.2:g.757280C>G

Transcript Alleles

HGVS Amino-acid change
ENST00000307340.8:c.13936C>G MANE Select ENSP00000305941.3:p.Pro4646Ala
ENST00000674083.1:c.13936C>G ENSP00000501296.1:p.Pro4646Ala
ENST00000307340.7:c.13936C>G ENSP00000305941.3:p.Pro4646Ala
NM_206933.2:c.13936C>G NP_996816.2:p.Pro4646Ala
NM_206933.3:c.13936C>G NP_996816.2:p.Pro4646Ala
NM_206933.4:c.13936C>G MANE Select NP_996816.3:p.Pro4646Ala