Canonical Allele Identifier: CA400961395

Gene: USH1G

Linked Data

• ClinVar Variation Id: 2306648
• ClinVar RCV Id: RCV002870040
• MyVariant Identifiers: chr17:g.72915696T>G (hg19) ; chr17:g.74919601T>G (hg38)

Genomic Alleles

HGVS	Genome Assembly
NC_000017.11:g.74919601T>G , CM000679.2:g.74919601T>G	GRCh38
NC_000017.10:g.72915696T>G , CM000679.1:g.72915696T>G	GRCh37
NC_000017.9:g.70427291T>G	NCBI36
NG_007882.1:g.8656A>C
NG_033062.1:g.327T>G
NG_007882.2:g.8663A>C
NG_033062.2:g.327T>G

Transcript Alleles

HGVS	Amino-acid Change
ENST00000614341.5:c.1235A>C MANE Select	ENSP00000480279.1:p.Lys412Thr
ENST00000579243.1:c.*834A>C	ENSP00000462568.1:n.*834A>C
ENST00000614341.4:c.1235A>C	ENSP00000480279.1:p.Lys412Thr
NM_001282489.2:c.926A>C	NP_001269418.1:p.Lys309Thr
NM_173477.4:c.1235A>C	NP_775748.2:p.Lys412Thr
XM_011524296.1:c.926A>C	XP_011522598.1:p.Lys309Thr
XM_011524296.2:c.926A>C	XP_011522598.1:p.Lys309Thr
NM_173477.5:c.1235A>C MANE Select	NP_775748.2:p.Lys412Thr
NM_001282489.3:c.926A>C	NP_001269418.1:p.Lys309Thr