Canonical Allele Identifier: CA2275255318
Gene: USH1G HGNC NCBI

Genomic Alleles

HGVS Genome Assembly
NC_000017.11:g.74919887A= , CM000679.2:g.74919887A= GRCh38
NC_000017.10:g.72915982A= , CM000679.1:g.72915982A= GRCh37
NC_000017.9:g.70427577A= NCBI36
NG_007882.1:g.8370T=
NG_033062.1:g.613A=
NG_007882.2:g.8377T=
NG_033062.2:g.613A=

Transcript Alleles

HGVS Amino-acid Change
ENST00000614341.5:c.949T= MANE Select ENSP00000480279.1:p.Phe317=
ENST00000579243.1:c.*548T= ENSP00000462568.1:n.*548T=
ENST00000614341.4:c.949T= ENSP00000480279.1:p.Phe317=
NM_001282489.2:c.640T= NP_001269418.1:p.Phe214=
NM_173477.4:c.949T= NP_775748.2:p.Phe317=
XM_011524296.1:c.640T= XP_011522598.1:p.Phe214=
XM_011524296.2:c.640T= XP_011522598.1:p.Phe214=
NM_173477.5:c.949T= MANE Select NP_775748.2:p.Phe317=
NM_001282489.3:c.640T= NP_001269418.1:p.Phe214=