Canonical Allele Identifier: CA502036700

Gene: USH1G

Linked Data

• MyVariant Identifiers: chr17:g.72916013C>A (hg19)

Genomic Alleles

HGVS	Genome Assembly
NC_000017.11:g.74919918C>A , CM000679.2:g.74919918C>A	GRCh38
NC_000017.10:g.72916013C>A , CM000679.1:g.72916013C>A	GRCh37
NC_000017.9:g.70427608C>A	NCBI36
NG_007882.1:g.8339G>T
NG_033062.1:g.644C>A
NG_007882.2:g.8346G>T
NG_033062.2:g.644C>A

Transcript Alleles

HGVS	Amino-acid Change
ENST00000614341.5:c.918G>T MANE Select	ENSP00000480279.1:p.Leu306=
ENST00000579243.1:c.*517G>T	ENSP00000462568.1:n.*517G>T
ENST00000614341.4:c.918G>T	ENSP00000480279.1:p.Leu306=
NM_001282489.2:c.609G>T	NP_001269418.1:p.Leu203=
NM_173477.4:c.918G>T	NP_775748.2:p.Leu306=
XM_011524296.1:c.609G>T	XP_011522598.1:p.Leu203=
XM_011524296.2:c.609G>T	XP_011522598.1:p.Leu203=
NM_173477.5:c.918G>T MANE Select	NP_775748.2:p.Leu306=
NM_001282489.3:c.609G>T	NP_001269418.1:p.Leu203=