Canonical Allele Identifier: CA400961434

Gene: USH1G

Linked Data

• dbSNP Id: rs2038908722
• MyVariant Identifiers: chr17:g.72915715C>T (hg19) ; chr17:g.74919620C>T (hg38)

Genomic Alleles

HGVS	Genome Assembly
NC_000017.11:g.74919620C>T , CM000679.2:g.74919620C>T	GRCh38
NC_000017.10:g.72915715C>T , CM000679.1:g.72915715C>T	GRCh37
NC_000017.9:g.70427310C>T	NCBI36
NG_007882.1:g.8637G>A
NG_033062.1:g.346C>T
NG_007882.2:g.8644G>A
NG_033062.2:g.346C>T

Transcript Alleles

HGVS	Amino-acid Change
ENST00000614341.5:c.1216G>A MANE Select	ENSP00000480279.1:p.Ala406Thr
ENST00000579243.1:c.*815G>A	ENSP00000462568.1:n.*815G>A
ENST00000614341.4:c.1216G>A	ENSP00000480279.1:p.Ala406Thr
NM_001282489.2:c.907G>A	NP_001269418.1:p.Ala303Thr
NM_173477.4:c.1216G>A	NP_775748.2:p.Ala406Thr
XM_011524296.1:c.907G>A	XP_011522598.1:p.Ala303Thr
XM_011524296.2:c.907G>A	XP_011522598.1:p.Ala303Thr
NM_173477.5:c.1216G>A MANE Select	NP_775748.2:p.Ala406Thr
NM_001282489.3:c.907G>A	NP_001269418.1:p.Ala303Thr