Canonical Allele Identifier: CA800383954

Gene: UNC5C

Linked Data

• dbSNP Id: rs1299730951
• gnomAD v3: 4-95537452-AAC-A
• MyVariant Identifiers: chr4:g.96458604_96458605del (hg19) ; chr4:g.95537453_95537454del (hg38)

Genomic Alleles

HGVS	Genome Assembly
NC_000004.12:g.95537458_95537459del , CM000666.2:g.95537458_95537459del	GRCh38
NC_000004.11:g.96458609_96458610del , CM000666.1:g.96458609_96458610del	GRCh37
NC_000004.10:g.96677632_96677633del	NCBI36

Transcript Alleles

HGVS	Amino-acid Change
ENST00000453304.6:c.124+11280_124+11281del MANE Select	ENSP00000406022.1:n.124+11280_124+11281del
ENST00000453304.5:c.124+11280_124+11281del	ENSP00000406022.1:n.124+11280_124+11281del
ENST00000504962.1:c.124+11280_124+11281del	ENSP00000425117.1:n.124+11280_124+11281del
ENST00000506749.5:c.124+11280_124+11281del	ENSP00000426153.1:n.124+11280_124+11281del
ENST00000513796.5:c.124+11280_124+11281del	ENSP00000426924.1:n.124+11280_124+11281del
NM_003728.3:c.124+11280_124+11281del	NP_003719.3:n.124+11280_124+11281del
XM_005263321.2:c.124+11280_124+11281del	XP_005263378.1:n.124+11280_124+11281del
XM_005263321.3:c.124+11280_124+11281del	XP_005263378.1:n.124+11280_124+11281del
NM_003728.4:c.124+11280_124+11281del MANE Select	NP_003719.3:n.124+11280_124+11281del