Canonical Allele Identifier: CA400964341

Gene: USH1G

Linked Data

• gnomAD v4: 17-74920226-C-A
• MyVariant Identifiers: chr17:g.72916321C>A (hg19) ; chr17:g.74920226C>A (hg38)

Genomic Alleles

HGVS	Genome Assembly
NC_000017.11:g.74920226C>A , CM000679.2:g.74920226C>A	GRCh38
NC_000017.10:g.72916321C>A , CM000679.1:g.72916321C>A	GRCh37
NC_000017.9:g.70427916C>A	NCBI36
NG_007882.1:g.8031G>T
NG_033062.1:g.952C>A
NG_007882.2:g.8038G>T
NG_033062.2:g.952C>A

Transcript Alleles

HGVS	Amino-acid Change
ENST00000614341.5:c.610G>T MANE Select	ENSP00000480279.1:p.Ala204Ser
ENST00000579243.1:c.*209G>T	ENSP00000462568.1:n.*209G>T
ENST00000614341.4:c.610G>T	ENSP00000480279.1:p.Ala204Ser
NM_001282489.2:c.301G>T	NP_001269418.1:p.Ala101Ser
NM_173477.4:c.610G>T	NP_775748.2:p.Ala204Ser
XM_011524296.1:c.301G>T	XP_011522598.1:p.Ala101Ser
XM_011524296.2:c.301G>T	XP_011522598.1:p.Ala101Ser
NM_173477.5:c.610G>T MANE Select	NP_775748.2:p.Ala204Ser
NM_001282489.3:c.301G>T	NP_001269418.1:p.Ala101Ser