Canonical Allele Identifier: CA1478149959
Gene: UNC5C HGNC NCBI

Genomic Alleles

HGVS Genome Assembly
NC_000004.12:g.95537237T= , CM000666.2:g.95537237T= GRCh38
NC_000004.11:g.96458388T= , CM000666.1:g.96458388T= GRCh37
NC_000004.10:g.96677411T= NCBI36

Transcript Alleles

HGVS Amino-acid change
ENST00000453304.6:c.124+11497A= MANE Select ENSP00000406022.1:n.124+11497A=
ENST00000453304.5:c.124+11497A= ENSP00000406022.1:n.124+11497A=
ENST00000504962.1:c.124+11497A= ENSP00000425117.1:n.124+11497A=
ENST00000506749.5:c.124+11497A= ENSP00000426153.1:n.124+11497A=
ENST00000513796.5:c.124+11497A= ENSP00000426924.1:n.124+11497A=
NM_003728.3:c.124+11497A= NP_003719.3:n.124+11497A=
XM_005263321.2:c.124+11497A= XP_005263378.1:n.124+11497A=
XM_005263321.3:c.124+11497A= XP_005263378.1:n.124+11497A=
NM_003728.4:c.124+11497A= MANE Select NP_003719.3:n.124+11497A=