Canonical Allele Identifier: CA2639748361
Gene: USH1G HGNC NCBI

Linked Data

Genomic Alleles

HGVS Genome Assembly
NC_000017.11:g.74922837T>C , CM000679.2:g.74922837T>C GRCh38
NC_000017.10:g.72918932T>C , CM000679.1:g.72918932T>C GRCh37
NC_000017.9:g.70430527T>C NCBI36
NG_007882.1:g.5420A>G
NG_033062.1:g.3563T>C
NG_007882.2:g.5427A>G
NG_033062.2:g.3563T>C

Transcript Alleles

HGVS Amino-acid change
ENST00000614341.5:c.164+73A>G MANE Select ENSP00000480279.1:n.164+73A>G
ENST00000579243.1:c.164+73A>G ENSP00000462568.1:n.164+73A>G
ENST00000614341.4:c.164+73A>G ENSP00000480279.1:n.164+73A>G
NM_001282489.2:c.-93+73A>G NP_001269418.1:n.-93+73A>G
NM_173477.4:c.164+73A>G NP_775748.2:n.164+73A>G
XM_011524296.1:c.-407A>G XP_011522598.1:n.-407A>G
XM_011524296.2:c.-407A>G XP_011522598.1:n.-407A>G
NM_173477.5:c.164+73A>G MANE Select NP_775748.2:n.164+73A>G
NM_001282489.3:c.-93+73A>G NP_001269418.1:n.-93+73A>G