Canonical Allele Identifier: CA1955186858

Gene: USH1C

Genomic Alleles

HGVS	Genome Assembly
NC_000011.10:g.17527006G= , CM000673.2:g.17527006G=	GRCh38
NC_000011.9:g.17548553G= , CM000673.1:g.17548553G=	GRCh37
NC_000011.8:g.17505129G=	NCBI36
NG_011883.1:g.22411C=
NG_011883.2:g.22411C=

Transcript Alleles

HGVS	Amino-acid Change
ENST00000005226.12:c.521+10C= MANE Select	ENSP00000005226.7:n.521+10C=
ENST00000318024.9:c.521+10C= MANE Plus Clinical	ENSP00000317018.4:n.521+10C=
ENST00000005226.11:c.521+10C=	ENSP00000005226.7:n.521+10C=
ENST00000318024.8:c.521+10C=	ENSP00000317018.4:n.521+10C=
ENST00000526181.1:c.554+10C=	ENSP00000437128.1:n.554+10C=
ENST00000526313.5:c.521+10C=	ENSP00000432236.1:n.521+10C=
ENST00000527020.5:c.521+10C=	ENSP00000436934.1:n.521+10C=
ENST00000527720.5:c.428+10C=	ENSP00000432944.1:n.428+10C=
NM_001297764.1:c.521+10C=	NP_001284693.1:n.521+10C=
NM_005709.3:c.521+10C=	NP_005700.2:n.521+10C=
NM_153676.3:c.521+10C=	NP_710142.1:n.521+10C=
NR_123738.1:n.630+10C=
XM_011519831.1:c.521+10C=	XP_011518133.1:n.521+10C=
XM_011519832.1:c.521+10C=	XP_011518134.1:n.521+10C=
XM_011519833.1:c.521+10C=	XP_011518135.1:n.521+10C=
XM_011519834.1:c.521+10C=	XP_011518136.1:n.521+10C=
XR_930841.1:n.630+10C=
XR_930842.1:n.630+10C=
XM_011519832.3:c.521+10C=	XP_011518134.1:n.521+10C=
XM_011519834.2:c.521+10C=	XP_011518136.1:n.521+10C=
XM_017017072.1:c.521+10C=	XP_016872561.1:n.521+10C=
XM_017017073.1:c.521+10C=	XP_016872562.1:n.521+10C=
XM_017017074.1:c.521+10C=	XP_016872563.1:n.521+10C=
XM_017017075.1:c.521+10C=	XP_016872564.1:n.521+10C=
XR_001747717.2:n.630+10C=
NM_153676.4:c.521+10C= MANE Select	NP_710142.1:n.521+10C=
NM_001297764.2:c.521+10C=	NP_001284693.1:n.521+10C=
NM_005709.4:c.521+10C= MANE Plus Clinical	NP_005700.2:n.521+10C=
NR_123738.2:n.630+10C=