Canonical Allele Identifier: CA400964252

Gene: USH1G

Linked Data

• MyVariant Identifiers: chr17:g.72916299C>T (hg19) ; chr17:g.74920204C>T (hg38)

Genomic Alleles

HGVS	Genome Assembly
NC_000017.11:g.74920204C>T , CM000679.2:g.74920204C>T	GRCh38
NC_000017.10:g.72916299C>T , CM000679.1:g.72916299C>T	GRCh37
NC_000017.9:g.70427894C>T	NCBI36
NG_007882.1:g.8053G>A
NG_033062.1:g.930C>T
NG_007882.2:g.8060G>A
NG_033062.2:g.930C>T

Transcript Alleles

HGVS	Amino-acid Change
ENST00000614341.5:c.632G>A MANE Select	ENSP00000480279.1:p.Arg211Lys
ENST00000579243.1:c.*231G>A	ENSP00000462568.1:n.*231G>A
ENST00000614341.4:c.632G>A	ENSP00000480279.1:p.Arg211Lys
NM_001282489.2:c.323G>A	NP_001269418.1:p.Arg108Lys
NM_173477.4:c.632G>A	NP_775748.2:p.Arg211Lys
XM_011524296.1:c.323G>A	XP_011522598.1:p.Arg108Lys
XM_011524296.2:c.323G>A	XP_011522598.1:p.Arg108Lys
NM_173477.5:c.632G>A MANE Select	NP_775748.2:p.Arg211Lys
NM_001282489.3:c.323G>A	NP_001269418.1:p.Arg108Lys