Canonical Allele Identifier: CA1478150013

Gene: UNC5C

Genomic Alleles

HGVS	Genome Assembly
NC_000004.12:g.95537368_95537370delinsAGG , CM000666.2:g.95537368_95537370delinsAGG	GRCh38
NC_000004.11:g.96458519_96458521delinsAGG , CM000666.1:g.96458519_96458521delinsAGG	GRCh37
NC_000004.10:g.96677542_96677544delinsAGG	NCBI36

Transcript Alleles

HGVS	Amino-acid Change
ENST00000453304.6:c.124+11364_124+11366delinsCCT MANE Select	ENSP00000406022.1:n.124+11364_124+11366delinsCCT
ENST00000453304.5:c.124+11364_124+11366delinsCCT	ENSP00000406022.1:n.124+11364_124+11366delinsCCT
ENST00000504962.1:c.124+11364_124+11366delinsCCT	ENSP00000425117.1:n.124+11364_124+11366delinsCCT
ENST00000506749.5:c.124+11364_124+11366delinsCCT	ENSP00000426153.1:n.124+11364_124+11366delinsCCT
ENST00000513796.5:c.124+11364_124+11366delinsCCT	ENSP00000426924.1:n.124+11364_124+11366delinsCCT
NM_003728.3:c.124+11364_124+11366delinsCCT	NP_003719.3:n.124+11364_124+11366delinsCCT
XM_005263321.2:c.124+11364_124+11366delinsCCT	XP_005263378.1:n.124+11364_124+11366delinsCCT
XM_005263321.3:c.124+11364_124+11366delinsCCT	XP_005263378.1:n.124+11364_124+11366delinsCCT
NM_003728.4:c.124+11364_124+11366delinsCCT MANE Select	NP_003719.3:n.124+11364_124+11366delinsCCT