Canonical Allele Identifier: CA344828369
Gene: USH2A HGNC NCBI

Linked Data

Genomic Alleles

HGVS Genome Assembly
NC_000001.11:g.215640696A>T , CM000663.2:g.215640696A>T GRCh38
NC_000001.10:g.215814038A>T , CM000663.1:g.215814038A>T GRCh37
NC_000001.9:g.213880661A>T NCBI36
NG_009497.1:g.787701T>A
NG_009497.2:g.787753T>A

Transcript Alleles

HGVS Amino-acid Change
ENST00000307340.8:c.14830T>A MANE Select ENSP00000305941.3:p.Leu4944Met
ENST00000674083.1:c.14830T>A ENSP00000501296.1:p.Leu4944Met
ENST00000307340.7:c.14830T>A ENSP00000305941.3:p.Leu4944Met
NM_206933.2:c.14830T>A NP_996816.2:p.Leu4944Met
NM_206933.3:c.14830T>A NP_996816.2:p.Leu4944Met
NM_206933.4:c.14830T>A MANE Select NP_996816.3:p.Leu4944Met