Canonical Allele Identifier: CA1478155421
Gene: UNC5C HGNC NCBI

Genomic Alleles

HGVS Genome Assembly
NC_000004.12:g.95546210A= , CM000666.2:g.95546210A= GRCh38
NC_000004.11:g.96467361A= , CM000666.1:g.96467361A= GRCh37
NC_000004.10:g.96686384A= NCBI36

Transcript Alleles

HGVS Amino-acid Change
ENST00000453304.6:c.124+2524T= MANE Select ENSP00000406022.1:n.124+2524T=
ENST00000453304.5:c.124+2524T= ENSP00000406022.1:n.124+2524T=
ENST00000504962.1:c.124+2524T= ENSP00000425117.1:n.124+2524T=
ENST00000506749.5:c.124+2524T= ENSP00000426153.1:n.124+2524T=
ENST00000513796.5:c.124+2524T= ENSP00000426924.1:n.124+2524T=
NM_003728.3:c.124+2524T= NP_003719.3:n.124+2524T=
XM_005263321.2:c.124+2524T= XP_005263378.1:n.124+2524T=
XM_005263321.3:c.124+2524T= XP_005263378.1:n.124+2524T=
NM_003728.4:c.124+2524T= MANE Select NP_003719.3:n.124+2524T=