Canonical Allele Identifier: CA502036812

Gene: USH1G

Linked Data

• gnomAD v4: 17-74920221-C-A
• MyVariant Identifiers: chr17:g.72916316C>A (hg19)

Genomic Alleles

HGVS	Genome Assembly
NC_000017.11:g.74920221C>A , CM000679.2:g.74920221C>A	GRCh38
NC_000017.10:g.72916316C>A , CM000679.1:g.72916316C>A	GRCh37
NC_000017.9:g.70427911C>A	NCBI36
NG_007882.1:g.8036G>T
NG_033062.1:g.947C>A
NG_007882.2:g.8043G>T
NG_033062.2:g.947C>A

Transcript Alleles

HGVS	Amino-acid Change
ENST00000614341.5:c.615G>T MANE Select	ENSP00000480279.1:p.Thr205=
ENST00000579243.1:c.*214G>T	ENSP00000462568.1:n.*214G>T
ENST00000614341.4:c.615G>T	ENSP00000480279.1:p.Thr205=
NM_001282489.2:c.306G>T	NP_001269418.1:p.Thr102=
NM_173477.4:c.615G>T	NP_775748.2:p.Thr205=
XM_011524296.1:c.306G>T	XP_011522598.1:p.Thr102=
XM_011524296.2:c.306G>T	XP_011522598.1:p.Thr102=
NM_173477.5:c.615G>T MANE Select	NP_775748.2:p.Thr205=
NM_001282489.3:c.306G>T	NP_001269418.1:p.Thr102=