Canonical Allele Identifier: CA400964156

Gene: USH1G

Linked Data

• MyVariant Identifiers: chr17:g.72916287T>A (hg19) ; chr17:g.74920192T>A (hg38)

Genomic Alleles

HGVS	Genome Assembly
NC_000017.11:g.74920192T>A , CM000679.2:g.74920192T>A	GRCh38
NC_000017.10:g.72916287T>A , CM000679.1:g.72916287T>A	GRCh37
NC_000017.9:g.70427882T>A	NCBI36
NG_007882.1:g.8065A>T
NG_033062.1:g.918T>A
NG_007882.2:g.8072A>T
NG_033062.2:g.918T>A

Transcript Alleles

HGVS	Amino-acid Change
ENST00000614341.5:c.644A>T MANE Select	ENSP00000480279.1:p.Lys215Met
ENST00000579243.1:c.*243A>T	ENSP00000462568.1:n.*243A>T
ENST00000614341.4:c.644A>T	ENSP00000480279.1:p.Lys215Met
NM_001282489.2:c.335A>T	NP_001269418.1:p.Lys112Met
NM_173477.4:c.644A>T	NP_775748.2:p.Lys215Met
XM_011524296.1:c.335A>T	XP_011522598.1:p.Lys112Met
XM_011524296.2:c.335A>T	XP_011522598.1:p.Lys112Met
NM_173477.5:c.644A>T MANE Select	NP_775748.2:p.Lys215Met
NM_001282489.3:c.335A>T	NP_001269418.1:p.Lys112Met