Canonical Allele Identifier: CA400964374

Gene: USH1G

Linked Data

• MyVariant Identifiers: chr17:g.72916329T>A (hg19) ; chr17:g.74920234T>A (hg38)

Genomic Alleles

HGVS	Genome Assembly
NC_000017.11:g.74920234T>A , CM000679.2:g.74920234T>A	GRCh38
NC_000017.10:g.72916329T>A , CM000679.1:g.72916329T>A	GRCh37
NC_000017.9:g.70427924T>A	NCBI36
NG_007882.1:g.8023A>T
NG_033062.1:g.960T>A
NG_007882.2:g.8030A>T
NG_033062.2:g.960T>A

Transcript Alleles

HGVS	Amino-acid Change
ENST00000614341.5:c.602A>T MANE Select	ENSP00000480279.1:p.Tyr201Phe
ENST00000579243.1:c.*201A>T	ENSP00000462568.1:n.*201A>T
ENST00000614341.4:c.602A>T	ENSP00000480279.1:p.Tyr201Phe
NM_001282489.2:c.293A>T	NP_001269418.1:p.Tyr98Phe
NM_173477.4:c.602A>T	NP_775748.2:p.Tyr201Phe
XM_011524296.1:c.293A>T	XP_011522598.1:p.Tyr98Phe
XM_011524296.2:c.293A>T	XP_011522598.1:p.Tyr98Phe
NM_173477.5:c.602A>T MANE Select	NP_775748.2:p.Tyr201Phe
NM_001282489.3:c.293A>T	NP_001269418.1:p.Tyr98Phe