Canonical Allele Identifier: CA1955173296

Gene: USH1C

Genomic Alleles

HGVS	Genome Assembly
NC_000011.10:g.17501232A= , CM000673.2:g.17501232A=	GRCh38
NC_000011.9:g.17522779A= , CM000673.1:g.17522779A=	GRCh37
NC_000011.8:g.17479355A=	NCBI36
NG_011883.1:g.48185T=
NG_011883.2:g.48185T=

Transcript Alleles

HGVS	Amino-acid Change
ENST00000005226.12:c.2281-82T= MANE Select	ENSP00000005226.7:n.2281-82T=
ENST00000318024.9:c.1381-82T= MANE Plus Clinical	ENSP00000317018.4:n.1381-82T=
ENST00000005226.11:c.2281-82T=	ENSP00000005226.7:n.2281-82T=
ENST00000318024.8:c.1381-82T=	ENSP00000317018.4:n.1381-82T=
ENST00000526313.5:c.*95-82T=	ENSP00000432236.1:n.*95-82T=
ENST00000527020.5:c.1324-82T=	ENSP00000436934.1:n.1324-82T=
ENST00000527720.5:c.1288-82T=	ENSP00000432944.1:n.1288-82T=
ENST00000529563.5:n.265-82T=
ENST00000534556.1:n.166-82T=
NM_001297764.1:c.1324-82T=	NP_001284693.1:n.1324-82T=
NM_005709.3:c.1381-82T=	NP_005700.2:n.1381-82T=
NM_153676.3:c.2281-82T=	NP_710142.1:n.2281-82T=
NR_123738.1:n.1416-82T=
XM_011519831.1:c.2305-82T=	XP_011518133.1:n.2305-82T=
XM_011519832.1:c.1534-82T=	XP_011518134.1:n.1534-82T=
XM_011519833.1:c.1431-82T=	XP_011518135.1:n.1431-82T=
XR_930841.1:n.1752-82T=
XR_930842.1:n.1693-82T=
XM_011519832.3:c.1534-82T=	XP_011518134.1:n.1534-82T=
XM_017017075.1:c.2281-82T=	XP_016872564.1:n.2281-82T=
XR_001747717.2:n.1540-82T=
NM_153676.4:c.2281-82T= MANE Select	NP_710142.1:n.2281-82T=
NM_001297764.2:c.1324-82T=	NP_001284693.1:n.1324-82T=
NM_005709.4:c.1381-82T= MANE Plus Clinical	NP_005700.2:n.1381-82T=
NR_123738.2:n.1416-82T=