Canonical Allele Identifier: CA553475568
Gene: UNC5C HGNC NCBI

Linked Data

dbSNP Id: rs1158789321
gnomAD v2: 4-96458271-G-GT
gnomAD v3: 4-95537120-G-GT
gnomAD v4: 4-95537120-G-GT
MyVariant Identifiers: chr4:g.96458272_96458273insT (hg19) chr4:g.96458271_96458272insT (hg19) chr4:g.95537121_95537122insT (hg38) chr4:g.95537120_95537121insT (hg38)
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Genomic Alleles

HGVS Genome Assembly
NC_000004.12:g.95537129dup , CM000666.2:g.95537129dup GRCh38
NC_000004.11:g.96458280dup , CM000666.1:g.96458280dup GRCh37
NC_000004.10:g.96677303dup NCBI36

Transcript Alleles

HGVS Amino-acid change
ENST00000453304.6:c.124+11613dup MANE Select ENSP00000406022.1:n.124+11613dup
ENST00000453304.5:c.124+11613dup ENSP00000406022.1:n.124+11613dup
ENST00000504962.1:c.124+11613dup ENSP00000425117.1:n.124+11613dup
ENST00000506749.5:c.124+11613dup ENSP00000426153.1:n.124+11613dup
ENST00000513796.5:c.124+11613dup ENSP00000426924.1:n.124+11613dup
NM_003728.3:c.124+11613dup NP_003719.3:n.124+11613dup
XM_005263321.2:c.124+11613dup XP_005263378.1:n.124+11613dup
XM_005263321.3:c.124+11613dup XP_005263378.1:n.124+11613dup
NM_003728.4:c.124+11613dup MANE Select NP_003719.3:n.124+11613dup
Search 100 bp 5'
Search 100 bp 3'