Canonical Allele Identifier: CA400961351
Gene: USH1G HGNC NCBI

Linked Data

Genomic Alleles

HGVS Genome Assembly
NC_000017.11:g.74919580A>T , CM000679.2:g.74919580A>T GRCh38
NC_000017.10:g.72915675A>T , CM000679.1:g.72915675A>T GRCh37
NC_000017.9:g.70427270A>T NCBI36
NG_007882.1:g.8677T>A
NG_033062.1:g.306A>T
NG_007882.2:g.8684T>A
NG_033062.2:g.306A>T

Transcript Alleles

HGVS Amino-acid Change
ENST00000614341.5:c.1256T>A MANE Select ENSP00000480279.1:p.Met419Lys
ENST00000579243.1:c.*855T>A ENSP00000462568.1:n.*855T>A
ENST00000614341.4:c.1256T>A ENSP00000480279.1:p.Met419Lys
NM_001282489.2:c.947T>A NP_001269418.1:p.Met316Lys
NM_173477.4:c.1256T>A NP_775748.2:p.Met419Lys
XM_011524296.1:c.947T>A XP_011522598.1:p.Met316Lys
XM_011524296.2:c.947T>A XP_011522598.1:p.Met316Lys
NM_173477.5:c.1256T>A MANE Select NP_775748.2:p.Met419Lys
NM_001282489.3:c.947T>A NP_001269418.1:p.Met316Lys