Canonical Allele Identifier: CA400963301
Gene: USH1G HGNC NCBI

Linked Data

Genomic Alleles

HGVS Genome Assembly
NC_000017.11:g.74920048T>C , CM000679.2:g.74920048T>C GRCh38
NC_000017.10:g.72916143T>C , CM000679.1:g.72916143T>C GRCh37
NC_000017.9:g.70427738T>C NCBI36
NG_007882.1:g.8209A>G
NG_033062.1:g.774T>C
NG_007882.2:g.8216A>G
NG_033062.2:g.774T>C

Transcript Alleles

HGVS Amino-acid Change
ENST00000614341.5:c.788A>G MANE Select ENSP00000480279.1:p.Asn263Ser
ENST00000579243.1:c.*387A>G ENSP00000462568.1:n.*387A>G
ENST00000614341.4:c.788A>G ENSP00000480279.1:p.Asn263Ser
NM_001282489.2:c.479A>G NP_001269418.1:p.Asn160Ser
NM_173477.4:c.788A>G NP_775748.2:p.Asn263Ser
XM_011524296.1:c.479A>G XP_011522598.1:p.Asn160Ser
XM_011524296.2:c.479A>G XP_011522598.1:p.Asn160Ser
NM_173477.5:c.788A>G MANE Select NP_775748.2:p.Asn263Ser
NM_001282489.3:c.479A>G NP_001269418.1:p.Asn160Ser