Canonical Allele Identifier: CA400963815
Gene: USH1G HGNC NCBI

Linked Data

Genomic Alleles

HGVS Genome Assembly
NC_000017.11:g.74920140C>G , CM000679.2:g.74920140C>G GRCh38
NC_000017.10:g.72916235C>G , CM000679.1:g.72916235C>G GRCh37
NC_000017.9:g.70427830C>G NCBI36
NG_007882.1:g.8117G>C
NG_033062.1:g.866C>G
NG_007882.2:g.8124G>C
NG_033062.2:g.866C>G

Transcript Alleles

HGVS Amino-acid Change
ENST00000614341.5:c.696G>C MANE Select ENSP00000480279.1:p.Lys232Asn
ENST00000579243.1:c.*295G>C ENSP00000462568.1:n.*295G>C
ENST00000614341.4:c.696G>C ENSP00000480279.1:p.Lys232Asn
NM_001282489.2:c.387G>C NP_001269418.1:p.Lys129Asn
NM_173477.4:c.696G>C NP_775748.2:p.Lys232Asn
XM_011524296.1:c.387G>C XP_011522598.1:p.Lys129Asn
XM_011524296.2:c.387G>C XP_011522598.1:p.Lys129Asn
NM_173477.5:c.696G>C MANE Select NP_775748.2:p.Lys232Asn
NM_001282489.3:c.387G>C NP_001269418.1:p.Lys129Asn