Canonical Allele Identifier: CA473516424

Gene: USH1C

Linked Data

• dbSNP Id: rs1476715971
• gnomAD v4: 11-17509473-G-A
• MyVariant Identifiers: chr11:g.17531020G>A (hg19) ; chr11:g.17509473G>A (hg38)

Genomic Alleles

HGVS	Genome Assembly
NC_000011.10:g.17509473G>A , CM000673.2:g.17509473G>A	GRCh38
NC_000011.9:g.17531020G>A , CM000673.1:g.17531020G>A	GRCh37
NC_000011.8:g.17487596G>A	NCBI36
NG_011883.1:g.39944C>T
NG_011883.2:g.39944C>T

Transcript Alleles

HGVS	Amino-acid change
ENST00000005226.12:c.1896C>T MANE Select	ENSP00000005226.7:p.Asn632=
ENST00000318024.9:c.1285-7493C>T MANE Plus Clinical	ENSP00000317018.4:n.1285-7493C>T
ENST00000005226.11:c.1896C>T	ENSP00000005226.7:p.Asn632=
ENST00000318024.8:c.1285-7493C>T	ENSP00000317018.4:n.1285-7493C>T
ENST00000526313.5:c.1211-7493C>T	ENSP00000432236.1:n.1211-7493C>T
ENST00000527020.5:c.1228-7493C>T	ENSP00000436934.1:n.1228-7493C>T
ENST00000527720.5:c.1192-7493C>T	ENSP00000432944.1:n.1192-7493C>T
ENST00000529563.5:n.168+6982C>T
NM_001297764.1:c.1228-7493C>T	NP_001284693.1:n.1228-7493C>T
NM_005709.3:c.1285-7493C>T	NP_005700.2:n.1285-7493C>T
NM_153676.3:c.1896C>T	NP_710142.1:p.Asn632=
NR_123738.1:n.1320-7493C>T
XM_011519831.1:c.1920C>T	XP_011518133.1:p.Asn640=
XM_011519832.1:c.1437+2429C>T	XP_011518134.1:n.1437+2429C>T
XM_011519833.1:c.1334+6768C>T	XP_011518135.1:n.1334+6768C>T
XR_930841.1:n.1655+2429C>T
XR_930842.1:n.1596+2429C>T
XM_011519832.3:c.1437+2429C>T	XP_011518134.1:n.1437+2429C>T
XM_017017072.1:c.1920C>T	XP_016872561.1:p.Asn640=
XM_017017073.1:c.1863C>T	XP_016872562.1:p.Asn621=
XM_017017074.1:c.1555-244C>T	XP_016872563.1:n.1555-244C>T
XM_017017075.1:c.1896C>T	XP_016872564.1:p.Asn632=
XR_001747717.2:n.1443+6768C>T
NM_153676.4:c.1896C>T MANE Select	NP_710142.1:p.Asn632=
NM_001297764.2:c.1228-7493C>T	NP_001284693.1:n.1228-7493C>T
NM_005709.4:c.1285-7493C>T MANE Plus Clinical	NP_005700.2:n.1285-7493C>T
NR_123738.2:n.1320-7493C>T