Canonical Allele Identifier: CA2275254057
Gene: USH1G HGNC NCBI

Genomic Alleles

HGVS Genome Assembly
NC_000017.11:g.74917241C= , CM000679.2:g.74917241C= GRCh38
NC_000017.10:g.72913335C= , CM000679.1:g.72913335C= GRCh37
NC_000017.9:g.70424930C= NCBI36
NG_007882.1:g.11017G=
NG_007882.2:g.11023G=

Transcript Alleles

HGVS Amino-acid Change
ENST00000614341.5:c.*832G= MANE Select ENSP00000480279.1:n.*832G=
ENST00000614341.4:c.*832G= ENSP00000480279.1:n.*832G=
NM_001282489.2:c.*832G= NP_001269418.1:n.*832G=
NM_173477.4:c.*832G= NP_775748.2:n.*832G=
XM_011524296.1:c.*832G= XP_011522598.1:n.*832G=
XM_011524296.2:c.*832G= XP_011522598.1:n.*832G=
NM_173477.5:c.*832G= MANE Select NP_775748.2:n.*832G=
NM_001282489.3:c.*832G= NP_001269418.1:n.*832G=