Canonical Allele Identifier: CA344863038
Community Standard Title: NM_206933.4(USH2A):c.2994-2A>G
Gene: USH2A HGNC NCBI
USH2A-AS1 HGNC NCBI

Genomic Alleles

HGVS Genome Assembly
NC_000001.11:g.216217552T>C , CM000663.2:g.216217552T>C GRCh38
NC_000001.10:g.216390894T>C , CM000663.1:g.216390894T>C GRCh37
NC_000001.9:g.214457517T>C NCBI36
NG_009497.1:g.210845A>G
NG_009497.2:g.210897A>G

Transcript Alleles

HGVS Amino-acid Change
NM_206933.4:c.2994-2A>G (USH2A) MANE Select NP_996816.3:n.2994-2A>G
ENST00000307340.8:c.2994-2A>G (USH2A) MANE Select ENSP00000305941.3:n.2994-2A>G
NM_007123.5:c.2994-2A>G (USH2A) NP_009054.5:n.2994-2A>G
NM_007123.6:c.2994-2A>G (USH2A) NP_009054.6:n.2994-2A>G
NM_206933.2:c.2994-2A>G (USH2A) NP_996816.2:n.2994-2A>G
NM_206933.3:c.2994-2A>G (USH2A) NP_996816.2:n.2994-2A>G
ENST00000307340.7:c.2994-2A>G (USH2A) ENSP00000305941.3:n.2994-2A>G
ENST00000366942.3:c.2994-2A>G (USH2A) ENSP00000355909.3:n.2994-2A>G
ENST00000674083.1:c.2994-2A>G (USH2A) ENSP00000501296.1:n.2994-2A>G
XR_922596.1:n.355-7835T>C (USH2A-AS1)
XR_922596.3:n.1077-7835T>C (USH2A-AS1)
XR_922597.1:n.355-20283T>C (USH2A-AS1)