Canonical Allele Identifier: CA1478149999

Gene: UNC5C

Genomic Alleles

HGVS	Genome Assembly
NC_000004.12:g.95537336A= , CM000666.2:g.95537336A=	GRCh38
NC_000004.11:g.96458487A= , CM000666.1:g.96458487A=	GRCh37
NC_000004.10:g.96677510A=	NCBI36

Transcript Alleles

HGVS	Amino-acid change
ENST00000453304.6:c.124+11398T= MANE Select	ENSP00000406022.1:n.124+11398T=
ENST00000453304.5:c.124+11398T=	ENSP00000406022.1:n.124+11398T=
ENST00000504962.1:c.124+11398T=	ENSP00000425117.1:n.124+11398T=
ENST00000506749.5:c.124+11398T=	ENSP00000426153.1:n.124+11398T=
ENST00000513796.5:c.124+11398T=	ENSP00000426924.1:n.124+11398T=
NM_003728.3:c.124+11398T=	NP_003719.3:n.124+11398T=
XM_005263321.2:c.124+11398T=	XP_005263378.1:n.124+11398T=
XM_005263321.3:c.124+11398T=	XP_005263378.1:n.124+11398T=
NM_003728.4:c.124+11398T= MANE Select	NP_003719.3:n.124+11398T=