Canonical Allele Identifier: CA2747740492

Gene: USH2A

Genomic Alleles

HGVS	Genome Assembly
NC_000001.11:g.216418704_216418705del , CM000663.2:g.216418704_216418705del	GRCh38
NC_000001.10:g.216592046_216592047del , CM000663.1:g.216592046_216592047del	GRCh37
NC_000001.9:g.214658669_214658670del	NCBI36
NG_009497.1:g.9697_9698del
NG_009497.2:g.9749_9750del

Transcript Alleles

HGVS	Amino-acid Change
ENST00000307340.8:c.486-21_486-20del MANE Select	ENSP00000305941.3:n.486-21_486-20del
ENST00000674083.1:c.486-21_486-20del	ENSP00000501296.1:n.486-21_486-20del
ENST00000307340.7:c.486-21_486-20del	ENSP00000305941.3:n.486-21_486-20del
ENST00000366942.3:c.486-21_486-20del	ENSP00000355909.3:n.486-21_486-20del
NM_007123.5:c.486-21_486-20del	NP_009054.5:n.486-21_486-20del
NM_206933.2:c.486-21_486-20del	NP_996816.2:n.486-21_486-20del
NM_206933.3:c.486-21_486-20del	NP_996816.2:n.486-21_486-20del
NM_007123.6:c.486-21_486-20del	NP_009054.6:n.486-21_486-20del
NM_206933.4:c.486-21_486-20del MANE Select	NP_996816.3:n.486-21_486-20del