Canonical Allele Identifier: CA1220652636

Gene: USH2A

Genomic Alleles

HGVS	Genome Assembly
NC_000001.11:g.216324702_216324703delinsCA , CM000663.2:g.216324702_216324703delinsCA	GRCh38
NC_000001.10:g.216498044_216498045delinsCA , CM000663.1:g.216498044_216498045delinsCA	GRCh37
NC_000001.9:g.214564667_214564668delinsCA	NCBI36
NG_009497.1:g.103694_103695delinsTG
NG_009497.2:g.103746_103747delinsTG

Transcript Alleles

HGVS	Amino-acid Change
ENST00000307340.8:c.1144-351_1144-350delinsTG MANE Select	ENSP00000305941.3:n.1144-351_1144-350delinsTG
ENST00000674083.1:c.1144-351_1144-350delinsTG	ENSP00000501296.1:n.1144-351_1144-350delinsTG
ENST00000307340.7:c.1144-351_1144-350delinsTG	ENSP00000305941.3:n.1144-351_1144-350delinsTG
ENST00000366942.3:c.1144-351_1144-350delinsTG	ENSP00000355909.3:n.1144-351_1144-350delinsTG
NM_007123.5:c.1144-351_1144-350delinsTG	NP_009054.5:n.1144-351_1144-350delinsTG
NM_206933.2:c.1144-351_1144-350delinsTG	NP_996816.2:n.1144-351_1144-350delinsTG
NM_206933.3:c.1144-351_1144-350delinsTG	NP_996816.2:n.1144-351_1144-350delinsTG
NM_007123.6:c.1144-351_1144-350delinsTG	NP_009054.6:n.1144-351_1144-350delinsTG
NM_206933.4:c.1144-351_1144-350delinsTG MANE Select	NP_996816.3:n.1144-351_1144-350delinsTG