Canonical Allele Identifier: CA1955171699

Gene: USH1C

Genomic Alleles

HGVS	Genome Assembly
NC_000011.10:g.17498165G= , CM000673.2:g.17498165G=	GRCh38
NC_000011.9:g.17519712G= , CM000673.1:g.17519712G=	GRCh37
NC_000011.8:g.17476288G=	NCBI36
NG_011883.1:g.51252C=
NG_011883.2:g.51252C=

Transcript Alleles

HGVS	Amino-acid Change
ENST00000005226.12:c.2487C= MANE Select	ENSP00000005226.7:p.Gly829=
ENST00000318024.9:c.1587C= MANE Plus Clinical	ENSP00000317018.4:p.Gly529=
ENST00000005226.11:c.2487C=	ENSP00000005226.7:p.Gly829=
ENST00000318024.8:c.1587C=	ENSP00000317018.4:p.Gly529=
ENST00000526313.5:c.*301C=	ENSP00000432236.1:n.*301C=
ENST00000527020.5:c.1530C=	ENSP00000436934.1:p.Gly510=
ENST00000527720.5:c.1494C=	ENSP00000432944.1:p.Gly498=
ENST00000529563.5:n.471C=
NM_001297764.1:c.1530C=	NP_001284693.1:p.Gly510=
NM_005709.3:c.1587C=	NP_005700.2:p.Gly529=
NM_153676.3:c.2487C=	NP_710142.1:p.Gly829=
NR_123738.1:n.1622C=
XM_011519831.1:c.2511C=	XP_011518133.1:p.Gly837=
XM_011519832.1:c.1740C=	XP_011518134.1:p.Gly580=
XM_011519832.3:c.1740C=	XP_011518134.1:p.Gly580=
XM_017017075.1:c.2487C=	XP_016872564.1:p.Gly829=
XR_001747717.2:n.1746C=
NM_153676.4:c.2487C= MANE Select	NP_710142.1:p.Gly829=
NM_001297764.2:c.1530C=	NP_001284693.1:p.Gly510=
NM_005709.4:c.1587C= MANE Plus Clinical	NP_005700.2:p.Gly529=
NR_123738.2:n.1622C=