Canonical Allele Identifier: CA101709413
Gene: UNC5C HGNC NCBI

Linked Data

dbSNP Id: rs12643654
gnomAD v2: 4-96159817-A-G
gnomAD v3: 4-95238666-A-G
gnomAD v4: 4-95238666-A-G

Genomic Alleles

HGVS Genome Assembly
NC_000004.12:g.95238666A>G , CM000666.2:g.95238666A>G GRCh38
NC_000004.11:g.96159817A>G , CM000666.1:g.96159817A>G GRCh37
NC_000004.10:g.96378840A>G NCBI36

Transcript Alleles

HGVS Amino-acid change
ENST00000453304.6:c.1108+3763T>C MANE Select ENSP00000406022.1:n.1108+3763T>C
ENST00000453304.5:c.1108+3763T>C ENSP00000406022.1:n.1108+3763T>C
ENST00000506749.5:c.1108+3763T>C ENSP00000426153.1:n.1108+3763T>C
ENST00000513796.5:c.1108+3763T>C ENSP00000426924.1:n.1108+3763T>C
ENST00000610318.4:c.985+3763T>C ENSP00000483905.1:n.985+3763T>C
NM_003728.3:c.1108+3763T>C NP_003719.3:n.1108+3763T>C
XM_005263321.2:c.1108+3763T>C XP_005263378.1:n.1108+3763T>C
XM_005263321.3:c.1108+3763T>C XP_005263378.1:n.1108+3763T>C
XM_017008789.1:c.7+3763T>C XP_016864278.1:n.7+3763T>C
XM_017008790.1:c.7+3763T>C XP_016864279.1:n.7+3763T>C
NM_003728.4:c.1108+3763T>C MANE Select NP_003719.3:n.1108+3763T>C