Canonical Allele Identifier: CA1478149952
Gene: UNC5C HGNC NCBI

Genomic Alleles

HGVS Genome Assembly
NC_000004.12:g.95537231A= , CM000666.2:g.95537231A= GRCh38
NC_000004.11:g.96458382A= , CM000666.1:g.96458382A= GRCh37
NC_000004.10:g.96677405A= NCBI36

Transcript Alleles

HGVS Amino-acid change
ENST00000453304.6:c.124+11503T= MANE Select ENSP00000406022.1:n.124+11503T=
ENST00000453304.5:c.124+11503T= ENSP00000406022.1:n.124+11503T=
ENST00000504962.1:c.124+11503T= ENSP00000425117.1:n.124+11503T=
ENST00000506749.5:c.124+11503T= ENSP00000426153.1:n.124+11503T=
ENST00000513796.5:c.124+11503T= ENSP00000426924.1:n.124+11503T=
NM_003728.3:c.124+11503T= NP_003719.3:n.124+11503T=
XM_005263321.2:c.124+11503T= XP_005263378.1:n.124+11503T=
XM_005263321.3:c.124+11503T= XP_005263378.1:n.124+11503T=
NM_003728.4:c.124+11503T= MANE Select NP_003719.3:n.124+11503T=