Canonical Allele Identifier: CA5904406

Gene: USH1C

Linked Data

• dbSNP Id: rs754365594
• ExAC: 11:17531006 G / T
• gnomAD v2: 11-17531006-G-T
• gnomAD v4: 11-17509459-G-T
• MyVariant Identifiers: chr11:g.17531006G>T (hg19) ; chr11:g.17509459G>T (hg38)

Genomic Alleles

HGVS	Genome Assembly
NC_000011.10:g.17509459G>T , CM000673.2:g.17509459G>T	GRCh38
NC_000011.9:g.17531006G>T , CM000673.1:g.17531006G>T	GRCh37
NC_000011.8:g.17487582G>T	NCBI36
NG_011883.1:g.39958C>A
NG_011883.2:g.39958C>A

Transcript Alleles

HGVS	Amino-acid Change
ENST00000005226.12:c.1910C>A MANE Select	ENSP00000005226.7:p.Thr637Asn
ENST00000318024.9:c.1285-7479C>A MANE Plus Clinical	ENSP00000317018.4:n.1285-7479C>A
ENST00000005226.11:c.1910C>A	ENSP00000005226.7:p.Thr637Asn
ENST00000318024.8:c.1285-7479C>A	ENSP00000317018.4:n.1285-7479C>A
ENST00000526313.5:c.1211-7479C>A	ENSP00000432236.1:n.1211-7479C>A
ENST00000527020.5:c.1228-7479C>A	ENSP00000436934.1:n.1228-7479C>A
ENST00000527720.5:c.1192-7479C>A	ENSP00000432944.1:n.1192-7479C>A
ENST00000529563.5:n.168+6996C>A
NM_001297764.1:c.1228-7479C>A	NP_001284693.1:n.1228-7479C>A
NM_005709.3:c.1285-7479C>A	NP_005700.2:n.1285-7479C>A
NM_153676.3:c.1910C>A	NP_710142.1:p.Thr637Asn
NR_123738.1:n.1320-7479C>A
XM_011519831.1:c.1934C>A	XP_011518133.1:p.Thr645Asn
XM_011519832.1:c.1437+2443C>A	XP_011518134.1:n.1437+2443C>A
XM_011519833.1:c.1334+6782C>A	XP_011518135.1:n.1334+6782C>A
XR_930841.1:n.1655+2443C>A
XR_930842.1:n.1596+2443C>A
XM_011519832.3:c.1437+2443C>A	XP_011518134.1:n.1437+2443C>A
XM_017017072.1:c.1934C>A	XP_016872561.1:p.Thr645Asn
XM_017017073.1:c.1877C>A	XP_016872562.1:p.Thr626Asn
XM_017017074.1:c.1555-230C>A	XP_016872563.1:n.1555-230C>A
XM_017017075.1:c.1910C>A	XP_016872564.1:p.Thr637Asn
XR_001747717.2:n.1443+6782C>A
NM_153676.4:c.1910C>A MANE Select	NP_710142.1:p.Thr637Asn
NM_001297764.2:c.1228-7479C>A	NP_001284693.1:n.1228-7479C>A
NM_005709.4:c.1285-7479C>A MANE Plus Clinical	NP_005700.2:n.1285-7479C>A
NR_123738.2:n.1320-7479C>A