Canonical Allele Identifier: CA1478149958

Gene: UNC5C

Linked Data

• dbSNP Id: rs1722804359

Genomic Alleles

HGVS	Genome Assembly
NC_000004.12:g.95537238_95537240del , CM000666.2:g.95537238_95537240del	GRCh38
NC_000004.11:g.96458389_96458391del , CM000666.1:g.96458389_96458391del	GRCh37
NC_000004.10:g.96677412_96677414del	NCBI36

Transcript Alleles

HGVS	Amino-acid change
ENST00000453304.6:c.124+11496_124+11498del MANE Select	ENSP00000406022.1:n.124+11496_124+11498de...
ENST00000453304.5:c.124+11496_124+11498del	ENSP00000406022.1:n.124+11496_124+11498de...
ENST00000504962.1:c.124+11496_124+11498del	ENSP00000425117.1:n.124+11496_124+11498de...
ENST00000506749.5:c.124+11496_124+11498del	ENSP00000426153.1:n.124+11496_124+11498de...
ENST00000513796.5:c.124+11496_124+11498del	ENSP00000426924.1:n.124+11496_124+11498de...
NM_003728.3:c.124+11496_124+11498del	NP_003719.3:n.124+11496_124+11498del
XM_005263321.2:c.124+11496_124+11498del	XP_005263378.1:n.124+11496_124+11498del
XM_005263321.3:c.124+11496_124+11498del	XP_005263378.1:n.124+11496_124+11498del
NM_003728.4:c.124+11496_124+11498del MANE Select	NP_003719.3:n.124+11496_124+11498del