Canonical Allele Identifier: CA1478011927

Gene: UNC5C

Genomic Alleles

HGVS	Genome Assembly
NC_000004.12:g.95238666A= , CM000666.2:g.95238666A=	GRCh38
NC_000004.11:g.96159817A= , CM000666.1:g.96159817A=	GRCh37
NC_000004.10:g.96378840A=	NCBI36

Transcript Alleles

HGVS	Amino-acid Change
NM_003728.4:c.1108+3763T= MANE Select	NP_003719.3:n.1108+3763T=
ENST00000453304.6:c.1108+3763T= MANE Select	ENSP00000406022.1:n.1108+3763T=
NM_003728.3:c.1108+3763T=	NP_003719.3:n.1108+3763T=
ENST00000453304.5:c.1108+3763T=	ENSP00000406022.1:n.1108+3763T=
ENST00000506749.5:c.1108+3763T=	ENSP00000426153.1:n.1108+3763T=
ENST00000513796.5:c.1108+3763T=	ENSP00000426924.1:n.1108+3763T=
ENST00000610318.4:c.985+3763T=	ENSP00000483905.1:n.985+3763T=
XM_005263321.2:c.1108+3763T=	XP_005263378.1:n.1108+3763T=
XM_005263321.3:c.1108+3763T=	XP_005263378.1:n.1108+3763T=
XM_017008789.1:c.7+3763T=	XP_016864278.1:n.7+3763T=
XM_017008790.1:c.7+3763T=	XP_016864279.1:n.7+3763T=