Canonical Allele Identifier: CA2747717483
Gene: USH2A HGNC NCBI

Genomic Alleles

HGVS Genome Assembly
NC_000001.11:g.215671339_215671340insAG , CM000663.2:g.215671339_215671340insAG GRCh38
NC_000001.10:g.215844681_215844682insAG , CM000663.1:g.215844681_215844682insAG GRCh37
NC_000001.9:g.213911304_213911305insAG NCBI36
NG_009497.1:g.757057_757058insCT
NG_009497.2:g.757109_757110insCT

Transcript Alleles

HGVS Amino-acid Change
ENST00000307340.8:c.13812-47_13812-46insCT MANE Select ENSP00000305941.3:n.13812-47_13812-46insCT
ENST00000674083.1:c.13812-47_13812-46insCT ENSP00000501296.1:n.13812-47_13812-46insCT
ENST00000307340.7:c.13812-47_13812-46insCT ENSP00000305941.3:n.13812-47_13812-46insCT
NM_206933.2:c.13812-47_13812-46insCT NP_996816.2:n.13812-47_13812-46insCT
NM_206933.3:c.13812-47_13812-46insCT NP_996816.2:n.13812-47_13812-46insCT
NM_206933.4:c.13812-47_13812-46insCT MANE Select NP_996816.3:n.13812-47_13812-46insCT