Canonical Allele Identifier: CA1478150014
Gene: UNC5C HGNC NCBI

Linked Data

dbSNP Id: rs1722806880

Genomic Alleles

HGVS Genome Assembly
NC_000004.12:g.95537371_95537372del , CM000666.2:g.95537371_95537372del GRCh38
NC_000004.11:g.96458522_96458523del , CM000666.1:g.96458522_96458523del GRCh37
NC_000004.10:g.96677545_96677546del NCBI36

Transcript Alleles

HGVS Amino-acid change
ENST00000453304.6:c.124+11364_124+11365del MANE Select ENSP00000406022.1:n.124+11364_124+11365de...
ENST00000453304.5:c.124+11364_124+11365del ENSP00000406022.1:n.124+11364_124+11365de...
ENST00000504962.1:c.124+11364_124+11365del ENSP00000425117.1:n.124+11364_124+11365de...
ENST00000506749.5:c.124+11364_124+11365del ENSP00000426153.1:n.124+11364_124+11365de...
ENST00000513796.5:c.124+11364_124+11365del ENSP00000426924.1:n.124+11364_124+11365de...
NM_003728.3:c.124+11364_124+11365del NP_003719.3:n.124+11364_124+11365del
XM_005263321.2:c.124+11364_124+11365del XP_005263378.1:n.124+11364_124+11365del
XM_005263321.3:c.124+11364_124+11365del XP_005263378.1:n.124+11364_124+11365del
NM_003728.4:c.124+11364_124+11365del MANE Select NP_003719.3:n.124+11364_124+11365del