Canonical Allele Identifier: CA1478149904
Gene: UNC5C HGNC NCBI

Genomic Alleles

HGVS Genome Assembly
NC_000004.12:g.95537120_95537121delinsGT , CM000666.2:g.95537120_95537121delinsGT GRCh38
NC_000004.11:g.96458271_96458272delinsGT , CM000666.1:g.96458271_96458272delinsGT GRCh37
NC_000004.10:g.96677294_96677295delinsGT NCBI36

Transcript Alleles

HGVS Amino-acid change
ENST00000453304.6:c.124+11613_124+11614delinsAC MANE Select ENSP00000406022.1:n.124+11613_124+11614de...
ENST00000453304.5:c.124+11613_124+11614delinsAC ENSP00000406022.1:n.124+11613_124+11614de...
ENST00000504962.1:c.124+11613_124+11614delinsAC ENSP00000425117.1:n.124+11613_124+11614de...
ENST00000506749.5:c.124+11613_124+11614delinsAC ENSP00000426153.1:n.124+11613_124+11614de...
ENST00000513796.5:c.124+11613_124+11614delinsAC ENSP00000426924.1:n.124+11613_124+11614de...
NM_003728.3:c.124+11613_124+11614delinsAC NP_003719.3:n.124+11613_124+11614delinsAC...
XM_005263321.2:c.124+11613_124+11614delinsAC XP_005263378.1:n.124+11613_124+11614delin...
XM_005263321.3:c.124+11613_124+11614delinsAC XP_005263378.1:n.124+11613_124+11614delin...
NM_003728.4:c.124+11613_124+11614delinsAC MANE Select NP_003719.3:n.124+11613_124+11614delinsAC...