Canonical Allele Identifier: CA2275253487
Gene: USH1G HGNC NCBI
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Genomic Alleles

HGVS Genome Assembly
NC_000017.11:g.74916214A= , CM000679.2:g.74916214A= GRCh38
NC_000017.10:g.72912306A= , CM000679.1:g.72912306A= GRCh37
NC_000017.9:g.70423901A= NCBI36
NG_007882.1:g.12046T=
NG_007882.2:g.12050T=

Transcript Alleles

HGVS Amino-acid Change
ENST00000614341.5:c.*1859T= MANE Select ENSP00000480279.1:n.*1859T=
ENST00000614341.4:c.*1859T= ENSP00000480279.1:n.*1859T=
NM_001282489.2:c.*1859T= NP_001269418.1:n.*1859T=
NM_173477.4:c.*1859T= NP_775748.2:n.*1859T=
XM_011524296.1:c.*1859T= XP_011522598.1:n.*1859T=
XM_011524296.2:c.*1859T= XP_011522598.1:n.*1859T=
NM_173477.5:c.*1859T= MANE Select NP_775748.2:n.*1859T=
NM_001282489.3:c.*1859T= NP_001269418.1:n.*1859T=
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