Canonical Allele Identifier: CA1478150062

Gene: UNC5C

Genomic Alleles

HGVS	Genome Assembly
NC_000004.12:g.95537452_95537456delinsAACAC , CM000666.2:g.95537452_95537456delinsAACAC	GRCh38
NC_000004.11:g.96458603_96458607delinsAACAC , CM000666.1:g.96458603_96458607delinsAACAC	GRCh37
NC_000004.10:g.96677626_96677630delinsAACAC	NCBI36

Transcript Alleles

HGVS	Amino-acid Change
ENST00000453304.6:c.124+11278_124+11282delinsGTGTT MANE Select	ENSP00000406022.1:n.124+11278_124+11282delinsGTGTT
ENST00000453304.5:c.124+11278_124+11282delinsGTGTT	ENSP00000406022.1:n.124+11278_124+11282delinsGTGTT
ENST00000504962.1:c.124+11278_124+11282delinsGTGTT	ENSP00000425117.1:n.124+11278_124+11282delinsGTGTT
ENST00000506749.5:c.124+11278_124+11282delinsGTGTT	ENSP00000426153.1:n.124+11278_124+11282delinsGTGTT
ENST00000513796.5:c.124+11278_124+11282delinsGTGTT	ENSP00000426924.1:n.124+11278_124+11282delinsGTGTT
NM_003728.3:c.124+11278_124+11282delinsGTGTT	NP_003719.3:n.124+11278_124+11282delinsGTGTT
XM_005263321.2:c.124+11278_124+11282delinsGTGTT	XP_005263378.1:n.124+11278_124+11282delinsGTGTT
XM_005263321.3:c.124+11278_124+11282delinsGTGTT	XP_005263378.1:n.124+11278_124+11282delinsGTGTT
NM_003728.4:c.124+11278_124+11282delinsGTGTT MANE Select	NP_003719.3:n.124+11278_124+11282delinsGTGTT