Canonical Allele Identifier: CA2747738022

Gene: USH2A

Genomic Alleles

HGVS	Genome Assembly
NC_000001.11:g.216324408_216324409insCAG , CM000663.2:g.216324408_216324409insCAG	GRCh38
NC_000001.10:g.216497750_216497751insCAG , CM000663.1:g.216497750_216497751insCAG	GRCh37
NC_000001.9:g.214564373_214564374insCAG	NCBI36
NG_009497.1:g.103988_103989insCTG
NG_009497.2:g.104040_104041insCTG

Transcript Alleles

HGVS	Amino-acid Change
ENST00000307340.8:c.1144-57_1144-56insCTG MANE Select	ENSP00000305941.3:n.1144-57_1144-56insCTG
ENST00000674083.1:c.1144-57_1144-56insCTG	ENSP00000501296.1:n.1144-57_1144-56insCTG
ENST00000307340.7:c.1144-57_1144-56insCTG	ENSP00000305941.3:n.1144-57_1144-56insCTG
ENST00000366942.3:c.1144-57_1144-56insCTG	ENSP00000355909.3:n.1144-57_1144-56insCTG
NM_007123.5:c.1144-57_1144-56insCTG	NP_009054.5:n.1144-57_1144-56insCTG
NM_206933.2:c.1144-57_1144-56insCTG	NP_996816.2:n.1144-57_1144-56insCTG
NM_206933.3:c.1144-57_1144-56insCTG	NP_996816.2:n.1144-57_1144-56insCTG
NM_007123.6:c.1144-57_1144-56insCTG	NP_009054.6:n.1144-57_1144-56insCTG
NM_206933.4:c.1144-57_1144-56insCTG MANE Select	NP_996816.3:n.1144-57_1144-56insCTG