Canonical Allele Identifier: CA1065643463

Gene: UNC5C

Linked Data

• dbSNP Id: rs1560498434
• gnomAD v3: 4-95537376-G-T
• gnomAD v4: 4-95537376-G-T

Genomic Alleles

HGVS	Genome Assembly
NC_000004.12:g.95537376G>T , CM000666.2:g.95537376G>T	GRCh38
NC_000004.11:g.96458527G>T , CM000666.1:g.96458527G>T	GRCh37
NC_000004.10:g.96677550G>T	NCBI36

Transcript Alleles

HGVS	Amino-acid Change
ENST00000453304.6:c.124+11358C>A MANE Select	ENSP00000406022.1:n.124+11358C>A
ENST00000453304.5:c.124+11358C>A	ENSP00000406022.1:n.124+11358C>A
ENST00000504962.1:c.124+11358C>A	ENSP00000425117.1:n.124+11358C>A
ENST00000506749.5:c.124+11358C>A	ENSP00000426153.1:n.124+11358C>A
ENST00000513796.5:c.124+11358C>A	ENSP00000426924.1:n.124+11358C>A
NM_003728.3:c.124+11358C>A	NP_003719.3:n.124+11358C>A
XM_005263321.2:c.124+11358C>A	XP_005263378.1:n.124+11358C>A
XM_005263321.3:c.124+11358C>A	XP_005263378.1:n.124+11358C>A
NM_003728.4:c.124+11358C>A MANE Select	NP_003719.3:n.124+11358C>A