Canonical Allele Identifier: CA502036660

Gene: USH1G

Linked Data

• MyVariant Identifiers: chr17:g.72915764A>C (hg19)

Genomic Alleles

HGVS	Genome Assembly
NC_000017.11:g.74919669A>C , CM000679.2:g.74919669A>C	GRCh38
NC_000017.10:g.72915764A>C , CM000679.1:g.72915764A>C	GRCh37
NC_000017.9:g.70427359A>C	NCBI36
NG_007882.1:g.8588T>G
NG_033062.1:g.395A>C
NG_007882.2:g.8595T>G
NG_033062.2:g.395A>C

Transcript Alleles

HGVS	Amino-acid Change
ENST00000614341.5:c.1167T>G MANE Select	ENSP00000480279.1:p.Thr389=
ENST00000579243.1:c.*766T>G	ENSP00000462568.1:n.*766T>G
ENST00000614341.4:c.1167T>G	ENSP00000480279.1:p.Thr389=
NM_001282489.2:c.858T>G	NP_001269418.1:p.Thr286=
NM_173477.4:c.1167T>G	NP_775748.2:p.Thr389=
XM_011524296.1:c.858T>G	XP_011522598.1:p.Thr286=
XM_011524296.2:c.858T>G	XP_011522598.1:p.Thr286=
NM_173477.5:c.1167T>G MANE Select	NP_775748.2:p.Thr389=
NM_001282489.3:c.858T>G	NP_001269418.1:p.Thr286=