Canonical Allele Identifier: CA400961289

Gene: USH1G

Linked Data

• MyVariant Identifiers: chr17:g.72915646T>A (hg19) ; chr17:g.74919551T>A (hg38)

Genomic Alleles

HGVS	Genome Assembly
NC_000017.11:g.74919551T>A , CM000679.2:g.74919551T>A	GRCh38
NC_000017.10:g.72915646T>A , CM000679.1:g.72915646T>A	GRCh37
NC_000017.9:g.70427241T>A	NCBI36
NG_007882.1:g.8706A>T
NG_033062.1:g.277T>A
NG_007882.2:g.8713A>T
NG_033062.2:g.277T>A

Transcript Alleles

HGVS	Amino-acid Change
ENST00000614341.5:c.1285A>T MANE Select	ENSP00000480279.1:p.Ile429Phe
ENST00000579243.1:c.*884A>T	ENSP00000462568.1:n.*884A>T
ENST00000614341.4:c.1285A>T	ENSP00000480279.1:p.Ile429Phe
NM_001282489.2:c.976A>T	NP_001269418.1:p.Ile326Phe
NM_173477.4:c.1285A>T	NP_775748.2:p.Ile429Phe
XM_011524296.1:c.976A>T	XP_011522598.1:p.Ile326Phe
XM_011524296.2:c.976A>T	XP_011522598.1:p.Ile326Phe
NM_173477.5:c.1285A>T MANE Select	NP_775748.2:p.Ile429Phe
NM_001282489.3:c.976A>T	NP_001269418.1:p.Ile326Phe