Canonical Allele Identifier: CA1478150068

Gene: UNC5C

Linked Data

• dbSNP Id: rs1722810151

Genomic Alleles

HGVS	Genome Assembly
NC_000004.12:g.95537456C>T , CM000666.2:g.95537456C>T	GRCh38
NC_000004.11:g.96458607C>T , CM000666.1:g.96458607C>T	GRCh37
NC_000004.10:g.96677630C>T	NCBI36

Transcript Alleles

HGVS	Amino-acid Change
ENST00000453304.6:c.124+11278G>A MANE Select	ENSP00000406022.1:n.124+11278G>A
ENST00000453304.5:c.124+11278G>A	ENSP00000406022.1:n.124+11278G>A
ENST00000504962.1:c.124+11278G>A	ENSP00000425117.1:n.124+11278G>A
ENST00000506749.5:c.124+11278G>A	ENSP00000426153.1:n.124+11278G>A
ENST00000513796.5:c.124+11278G>A	ENSP00000426924.1:n.124+11278G>A
NM_003728.3:c.124+11278G>A	NP_003719.3:n.124+11278G>A
XM_005263321.2:c.124+11278G>A	XP_005263378.1:n.124+11278G>A
XM_005263321.3:c.124+11278G>A	XP_005263378.1:n.124+11278G>A
NM_003728.4:c.124+11278G>A MANE Select	NP_003719.3:n.124+11278G>A