Canonical Allele Identifier: CA1955173442

Gene: USH1C

Genomic Alleles

HGVS	Genome Assembly
NC_000011.10:g.17501490T= , CM000673.2:g.17501490T=	GRCh38
NC_000011.9:g.17523037T= , CM000673.1:g.17523037T=	GRCh37
NC_000011.8:g.17479613T=	NCBI36
NG_011883.1:g.47927A=
NG_011883.2:g.47927A=

Transcript Alleles

HGVS	Amino-acid Change
ENST00000005226.12:c.2272A= MANE Select	ENSP00000005226.7:p.Ile758=
ENST00000318024.9:c.1372A= MANE Plus Clinical	ENSP00000317018.4:p.Ile458=
ENST00000005226.11:c.2272A=	ENSP00000005226.7:p.Ile758=
ENST00000318024.8:c.1372A=	ENSP00000317018.4:p.Ile458=
ENST00000526313.5:c.*86A=	ENSP00000432236.1:n.*86A=
ENST00000527020.5:c.1315A=	ENSP00000436934.1:p.Ile439=
ENST00000527720.5:c.1279A=	ENSP00000432944.1:p.Ile427=
ENST00000529563.5:n.256A=
ENST00000534556.1:n.157A=
NM_001297764.1:c.1315A=	NP_001284693.1:p.Ile439=
NM_005709.3:c.1372A=	NP_005700.2:p.Ile458=
NM_153676.3:c.2272A=	NP_710142.1:p.Ile758=
NR_123738.1:n.1407A=
XM_011519831.1:c.2296A=	XP_011518133.1:p.Ile766=
XM_011519832.1:c.1525A=	XP_011518134.1:p.Ile509=
XM_011519833.1:c.1422A=	XP_011518135.1:p.Ala474=
XR_930841.1:n.1743A=
XR_930842.1:n.1684A=
XM_011519832.3:c.1525A=	XP_011518134.1:p.Ile509=
XM_017017075.1:c.2272A=	XP_016872564.1:p.Ile758=
XR_001747717.2:n.1531A=
NM_153676.4:c.2272A= MANE Select	NP_710142.1:p.Ile758=
NM_001297764.2:c.1315A=	NP_001284693.1:p.Ile439=
NM_005709.4:c.1372A= MANE Plus Clinical	NP_005700.2:p.Ile458=
NR_123738.2:n.1407A=