Canonical Allele Identifier: CA400964369

Gene: USH1G

Linked Data

• MyVariant Identifiers: chr17:g.72916327A>C (hg19) ; chr17:g.74920232A>C (hg38)

Genomic Alleles

HGVS	Genome Assembly
NC_000017.11:g.74920232A>C , CM000679.2:g.74920232A>C	GRCh38
NC_000017.10:g.72916327A>C , CM000679.1:g.72916327A>C	GRCh37
NC_000017.9:g.70427922A>C	NCBI36
NG_007882.1:g.8025T>G
NG_033062.1:g.958A>C
NG_007882.2:g.8032T>G
NG_033062.2:g.958A>C

Transcript Alleles

HGVS	Amino-acid Change
ENST00000614341.5:c.604T>G MANE Select	ENSP00000480279.1:p.Ser202Ala
ENST00000579243.1:c.*203T>G	ENSP00000462568.1:n.*203T>G
ENST00000614341.4:c.604T>G	ENSP00000480279.1:p.Ser202Ala
NM_001282489.2:c.295T>G	NP_001269418.1:p.Ser99Ala
NM_173477.4:c.604T>G	NP_775748.2:p.Ser202Ala
XM_011524296.1:c.295T>G	XP_011522598.1:p.Ser99Ala
XM_011524296.2:c.295T>G	XP_011522598.1:p.Ser99Ala
NM_173477.5:c.604T>G MANE Select	NP_775748.2:p.Ser202Ala
NM_001282489.3:c.295T>G	NP_001269418.1:p.Ser99Ala