Canonical Allele Identifier: CA1955177168

Gene: USH1C

Genomic Alleles

HGVS	Genome Assembly
NC_000011.10:g.17509539G= , CM000673.2:g.17509539G=	GRCh38
NC_000011.9:g.17531086G= , CM000673.1:g.17531086G=	GRCh37
NC_000011.8:g.17487662G=	NCBI36
NG_011883.1:g.39878C=
NG_011883.2:g.39878C=

Transcript Alleles

HGVS	Amino-acid Change
ENST00000005226.12:c.1830C= MANE Select	ENSP00000005226.7:p.Ser610=
ENST00000318024.9:c.1285-7559C= MANE Plus Clinical	ENSP00000317018.4:n.1285-7559C=
ENST00000005226.11:c.1830C=	ENSP00000005226.7:p.Ser610=
ENST00000318024.8:c.1285-7559C=	ENSP00000317018.4:n.1285-7559C=
ENST00000526313.5:c.1211-7559C=	ENSP00000432236.1:n.1211-7559C=
ENST00000527020.5:c.1228-7559C=	ENSP00000436934.1:n.1228-7559C=
ENST00000527720.5:c.1192-7559C=	ENSP00000432944.1:n.1192-7559C=
ENST00000529563.5:n.168+6916C=
NM_001297764.1:c.1228-7559C=	NP_001284693.1:n.1228-7559C=
NM_005709.3:c.1285-7559C=	NP_005700.2:n.1285-7559C=
NM_153676.3:c.1830C=	NP_710142.1:p.Ser610=
NR_123738.1:n.1320-7559C=
XM_011519831.1:c.1854C=	XP_011518133.1:p.Ser618=
XM_011519832.1:c.1437+2363C=	XP_011518134.1:n.1437+2363C=
XM_011519833.1:c.1334+6702C=	XP_011518135.1:n.1334+6702C=
XR_930841.1:n.1655+2363C=
XR_930842.1:n.1596+2363C=
XM_011519832.3:c.1437+2363C=	XP_011518134.1:n.1437+2363C=
XM_017017072.1:c.1854C=	XP_016872561.1:p.Ser618=
XM_017017073.1:c.1797C=	XP_016872562.1:p.Ser599=
XM_017017074.1:c.1555-310C=	XP_016872563.1:n.1555-310C=
XM_017017075.1:c.1830C=	XP_016872564.1:p.Ser610=
XR_001747717.2:n.1443+6702C=
NM_153676.4:c.1830C= MANE Select	NP_710142.1:p.Ser610=
NM_001297764.2:c.1228-7559C=	NP_001284693.1:n.1228-7559C=
NM_005709.4:c.1285-7559C= MANE Plus Clinical	NP_005700.2:n.1285-7559C=
NR_123738.2:n.1320-7559C=