Canonical Allele Identifier: CA1065643368

Gene: UNC5C

Linked Data

• dbSNP Id: rs1722799732

Genomic Alleles

HGVS	Genome Assembly
NC_000004.12:g.95537078_95537081del , CM000666.2:g.95537078_95537081del	GRCh38
NC_000004.11:g.96458229_96458232del , CM000666.1:g.96458229_96458232del	GRCh37
NC_000004.10:g.96677252_96677255del	NCBI36

Transcript Alleles

HGVS	Amino-acid Change
ENST00000453304.6:c.124+11657_124+11660del MANE Select	ENSP00000406022.1:n.124+11657_124+11660del
ENST00000453304.5:c.124+11657_124+11660del	ENSP00000406022.1:n.124+11657_124+11660del
ENST00000504962.1:c.124+11657_124+11660del	ENSP00000425117.1:n.124+11657_124+11660del
ENST00000506749.5:c.124+11657_124+11660del	ENSP00000426153.1:n.124+11657_124+11660del
ENST00000513796.5:c.124+11657_124+11660del	ENSP00000426924.1:n.124+11657_124+11660del
NM_003728.3:c.124+11657_124+11660del	NP_003719.3:n.124+11657_124+11660del
XM_005263321.2:c.124+11657_124+11660del	XP_005263378.1:n.124+11657_124+11660del
XM_005263321.3:c.124+11657_124+11660del	XP_005263378.1:n.124+11657_124+11660del
NM_003728.4:c.124+11657_124+11660del MANE Select	NP_003719.3:n.124+11657_124+11660del