Canonical Allele Identifier: CA2517011453
Gene: UNC5C HGNC NCBI
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Genomic Alleles

HGVS Genome Assembly
NC_000004.12:g.95546244G>A , CM000666.2:g.95546244G>A GRCh38
NC_000004.11:g.96467395G>A , CM000666.1:g.96467395G>A GRCh37
NC_000004.10:g.96686418G>A NCBI36

Transcript Alleles

HGVS Amino-acid change
ENST00000453304.6:c.124+2490C>T MANE Select ENSP00000406022.1:n.124+2490C>T
ENST00000453304.5:c.124+2490C>T ENSP00000406022.1:n.124+2490C>T
ENST00000504962.1:c.124+2490C>T ENSP00000425117.1:n.124+2490C>T
ENST00000506749.5:c.124+2490C>T ENSP00000426153.1:n.124+2490C>T
ENST00000513796.5:c.124+2490C>T ENSP00000426924.1:n.124+2490C>T
NM_003728.3:c.124+2490C>T NP_003719.3:n.124+2490C>T
XM_005263321.2:c.124+2490C>T XP_005263378.1:n.124+2490C>T
XM_005263321.3:c.124+2490C>T XP_005263378.1:n.124+2490C>T
NM_003728.4:c.124+2490C>T MANE Select NP_003719.3:n.124+2490C>T
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