Canonical Allele Identifier: CA1478150011
Gene: UNC5C HGNC NCBI
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Genomic Alleles

HGVS Genome Assembly
NC_000004.12:g.95537364G= , CM000666.2:g.95537364G= GRCh38
NC_000004.11:g.96458515G= , CM000666.1:g.96458515G= GRCh37
NC_000004.10:g.96677538G= NCBI36

Transcript Alleles

HGVS Amino-acid change
ENST00000453304.6:c.124+11370C= MANE Select ENSP00000406022.1:n.124+11370C=
ENST00000453304.5:c.124+11370C= ENSP00000406022.1:n.124+11370C=
ENST00000504962.1:c.124+11370C= ENSP00000425117.1:n.124+11370C=
ENST00000506749.5:c.124+11370C= ENSP00000426153.1:n.124+11370C=
ENST00000513796.5:c.124+11370C= ENSP00000426924.1:n.124+11370C=
NM_003728.3:c.124+11370C= NP_003719.3:n.124+11370C=
XM_005263321.2:c.124+11370C= XP_005263378.1:n.124+11370C=
XM_005263321.3:c.124+11370C= XP_005263378.1:n.124+11370C=
NM_003728.4:c.124+11370C= MANE Select NP_003719.3:n.124+11370C=
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