Canonical Allele Identifier: CA1720489533

Gene: SEMA3C

Genomic Alleles

HGVS	Genome Assembly
NC_000007.14:g.80902935_80902938delinsTAAG , CM000669.2:g.80902935_80902938delinsTAAG	GRCh38
NC_000007.13:g.80532251_80532254delinsTAAG , CM000669.1:g.80532251_80532254delinsTAAG	GRCh37
NC_000007.12:g.80370187_80370190delinsTAAG	NCBI36
NG_054744.1:g.24442_24445delinsCTTA

Transcript Alleles

HGVS	Amino-acid Change
ENST00000265361.8:c.103+13741_103+13744delinsCTTA MANE Select	ENSP00000265361.3:n.103+13741_103+13744delinsCTTA
ENST00000265361.7:c.103+13741_103+13744delinsCTTA	ENSP00000265361.3:n.103+13741_103+13744delinsCTTA
ENST00000411788.5:c.191+2891_191+2894delinsCTTA	ENSP00000395398.1:n.191+2891_191+2894delinsCTTA
ENST00000419255.6:c.103+13741_103+13744delinsCTTA	ENSP00000411193.2:n.103+13741_103+13744delinsCTTA
ENST00000427167.5:c.191+2891_191+2894delinsCTTA	ENSP00000399891.1:n.191+2891_191+2894delinsCTTA
ENST00000458729.5:c.103+13741_103+13744delinsCTTA	ENSP00000393825.1:n.103+13741_103+13744delinsCTTA
ENST00000487621.5:n.496+13741_496+13744delinsCTTA
NM_006379.3:c.103+13741_103+13744delinsCTTA	NP_006370.1:n.103+13741_103+13744delinsCTTA
XM_005250113.1:c.-72+2891_-72+2894delinsCTTA	XP_005250170.1:n.-72+2891_-72+2894delinsCTTA
NM_001350120.1:c.157+13741_157+13744delinsCTTA	NP_001337049.1:n.157+13741_157+13744delinsCTTA
NM_001350121.1:c.-72+2891_-72+2894delinsCTTA	NP_001337050.1:n.-72+2891_-72+2894delinsCTTA
NM_006379.4:c.103+13741_103+13744delinsCTTA	NP_006370.1:n.103+13741_103+13744delinsCTTA
NM_006379.5:c.103+13741_103+13744delinsCTTA MANE Select	NP_006370.1:n.103+13741_103+13744delinsCTTA
NM_001350120.2:c.157+13741_157+13744delinsCTTA	NP_001337049.1:n.157+13741_157+13744delinsCTTA
NM_001350121.2:c.-72+2891_-72+2894delinsCTTA	NP_001337050.1:n.-72+2891_-72+2894delinsCTTA