Canonical Allele Identifier: CA2747735807

Gene: USH2A

Genomic Alleles

HGVS	Genome Assembly
NC_000001.11:g.216247244_216247245insAGA , CM000663.2:g.216247244_216247245insAGA	GRCh38
NC_000001.10:g.216420586_216420587insAGA , CM000663.1:g.216420586_216420587insAGA	GRCh37
NC_000001.9:g.214487209_214487210insAGA	NCBI36
NG_009497.1:g.181152_181153insTCT
NG_009497.2:g.181204_181205insTCT

Transcript Alleles

HGVS	Amino-acid Change
ENST00000307340.8:c.2168-19_2168-18insTCT MANE Select	ENSP00000305941.3:n.2168-19_2168-18insTCT
ENST00000674083.1:c.2168-19_2168-18insTCT	ENSP00000501296.1:n.2168-19_2168-18insTCT
ENST00000307340.7:c.2168-19_2168-18insTCT	ENSP00000305941.3:n.2168-19_2168-18insTCT
ENST00000366942.3:c.2168-19_2168-18insTCT	ENSP00000355909.3:n.2168-19_2168-18insTCT
NM_007123.5:c.2168-19_2168-18insTCT	NP_009054.5:n.2168-19_2168-18insTCT
NM_206933.2:c.2168-19_2168-18insTCT	NP_996816.2:n.2168-19_2168-18insTCT
NM_206933.3:c.2168-19_2168-18insTCT	NP_996816.2:n.2168-19_2168-18insTCT
NM_007123.6:c.2168-19_2168-18insTCT	NP_009054.6:n.2168-19_2168-18insTCT
NM_206933.4:c.2168-19_2168-18insTCT MANE Select	NP_996816.3:n.2168-19_2168-18insTCT