Canonical Allele Identifier: CA2275255482
Gene: USH1G HGNC NCBI

Genomic Alleles

HGVS Genome Assembly
NC_000017.11:g.74920182C= , CM000679.2:g.74920182C= GRCh38
NC_000017.10:g.72916277C= , CM000679.1:g.72916277C= GRCh37
NC_000017.9:g.70427872C= NCBI36
NG_007882.1:g.8075G=
NG_033062.1:g.908C=
NG_007882.2:g.8082G=
NG_033062.2:g.908C=

Transcript Alleles

HGVS Amino-acid Change
ENST00000614341.5:c.654G= MANE Select ENSP00000480279.1:p.Lys218=
ENST00000579243.1:c.*253G= ENSP00000462568.1:n.*253G=
ENST00000614341.4:c.654G= ENSP00000480279.1:p.Lys218=
NM_001282489.2:c.345G= NP_001269418.1:p.Lys115=
NM_173477.4:c.654G= NP_775748.2:p.Lys218=
XM_011524296.1:c.345G= XP_011522598.1:p.Lys115=
XM_011524296.2:c.345G= XP_011522598.1:p.Lys115=
NM_173477.5:c.654G= MANE Select NP_775748.2:p.Lys218=
NM_001282489.3:c.345G= NP_001269418.1:p.Lys115=