Canonical Allele Identifier: CA400961956

Gene: USH1G

Linked Data

• MyVariant Identifiers: chr17:g.72915885G>T (hg19) ; chr17:g.74919790G>T (hg38)

Genomic Alleles

HGVS	Genome Assembly
NC_000017.11:g.74919790G>T , CM000679.2:g.74919790G>T	GRCh38
NC_000017.10:g.72915885G>T , CM000679.1:g.72915885G>T	GRCh37
NC_000017.9:g.70427480G>T	NCBI36
NG_007882.1:g.8467C>A
NG_033062.1:g.516G>T
NG_007882.2:g.8474C>A
NG_033062.2:g.516G>T

Transcript Alleles

HGVS	Amino-acid change
ENST00000614341.5:c.1046C>A MANE Select	ENSP00000480279.1:p.Ser349Tyr
ENST00000579243.1:c.*645C>A	ENSP00000462568.1:n.*645C>A
ENST00000614341.4:c.1046C>A	ENSP00000480279.1:p.Ser349Tyr
NM_001282489.2:c.737C>A	NP_001269418.1:p.Ser246Tyr
NM_173477.4:c.1046C>A	NP_775748.2:p.Ser349Tyr
XM_011524296.1:c.737C>A	XP_011522598.1:p.Ser246Tyr
XM_011524296.2:c.737C>A	XP_011522598.1:p.Ser246Tyr
NM_173477.5:c.1046C>A MANE Select	NP_775748.2:p.Ser349Tyr
NM_001282489.3:c.737C>A	NP_001269418.1:p.Ser246Tyr