Canonical Allele Identifier: CA2275255301
Gene: USH1G HGNC NCBI

Genomic Alleles

HGVS Genome Assembly
NC_000017.11:g.74919855G= , CM000679.2:g.74919855G= GRCh38
NC_000017.10:g.72915950G= , CM000679.1:g.72915950G= GRCh37
NC_000017.9:g.70427545G= NCBI36
NG_007882.1:g.8402C=
NG_033062.1:g.581G=
NG_007882.2:g.8409C=
NG_033062.2:g.581G=

Transcript Alleles

HGVS Amino-acid Change
ENST00000614341.5:c.981C= MANE Select ENSP00000480279.1:p.His327=
ENST00000579243.1:c.*580C= ENSP00000462568.1:n.*580C=
ENST00000614341.4:c.981C= ENSP00000480279.1:p.His327=
NM_001282489.2:c.672C= NP_001269418.1:p.His224=
NM_173477.4:c.981C= NP_775748.2:p.His327=
XM_011524296.1:c.672C= XP_011522598.1:p.His224=
XM_011524296.2:c.672C= XP_011522598.1:p.His224=
NM_173477.5:c.981C= MANE Select NP_775748.2:p.His327=
NM_001282489.3:c.672C= NP_001269418.1:p.His224=