Canonical Allele Identifier: CA400964216

Gene: USH1G

Linked Data

• MyVariant Identifiers: chr17:g.72916293T>A (hg19) ; chr17:g.74920198T>A (hg38)

Genomic Alleles

HGVS	Genome Assembly
NC_000017.11:g.74920198T>A , CM000679.2:g.74920198T>A	GRCh38
NC_000017.10:g.72916293T>A , CM000679.1:g.72916293T>A	GRCh37
NC_000017.9:g.70427888T>A	NCBI36
NG_007882.1:g.8059A>T
NG_033062.1:g.924T>A
NG_007882.2:g.8066A>T
NG_033062.2:g.924T>A

Transcript Alleles

HGVS	Amino-acid Change
ENST00000614341.5:c.638A>T MANE Select	ENSP00000480279.1:p.Lys213Met
ENST00000579243.1:c.*237A>T	ENSP00000462568.1:n.*237A>T
ENST00000614341.4:c.638A>T	ENSP00000480279.1:p.Lys213Met
NM_001282489.2:c.329A>T	NP_001269418.1:p.Lys110Met
NM_173477.4:c.638A>T	NP_775748.2:p.Lys213Met
XM_011524296.1:c.329A>T	XP_011522598.1:p.Lys110Met
XM_011524296.2:c.329A>T	XP_011522598.1:p.Lys110Met
NM_173477.5:c.638A>T MANE Select	NP_775748.2:p.Lys213Met
NM_001282489.3:c.329A>T	NP_001269418.1:p.Lys110Met