Canonical Allele Identifier: CA2519307990

Gene: SEMA3C

Genomic Alleles

HGVS	Genome Assembly
NC_000007.14:g.80902933_80902934insTGATGTTGTGATATCATGACGACATGTGTTTTGGTTTTAAATGAATCATTGATGTTAGTTAGT , CM000669.2:g.80902933_80902934insTGATGTTGTGATATCATGACGACATGTGTTTTGGTTTTAAATGAATCATTGATGTTAGTTAGT	GRCh38
NC_000007.13:g.80532249_80532250insTGATGTTGTGATATCATGACGACATGTGTTTTGGTTTTAAATGAATCATTGATGTTAGTTAGT , CM000669.1:g.80532249_80532250insTGATGTTGTGATATCATGACGACATGTGTTTTGGTTTTAAATGAATCATTGATGTTAGTTAGT	GRCh37
NC_000007.12:g.80370185_80370186insTGATGTTGTGATATCATGACGACATGTGTTTTGGTTTTAAATGAATCATTGATGTTAGTTAGT	NCBI36
NG_054744.1:g.24446_24447insACTAACTAACATCAATGATTCATTTAAAACCAAAACACATGTCGTCATGATATCACAACATCA

Transcript Alleles

HGVS	Amino-acid Change
ENST00000265361.8:c.103+13745_103+13746insACTAACTAACATCAATGATTCATTTAAAACCAAAACACATGTCGTCATGATATCACAACATCA MANE Select	ENSP00000265361.3:n.103+13745_103+13746insACTAACTAACATCAATGAT...
ENST00000265361.7:c.103+13745_103+13746insACTAACTAACATCAATGATTCATTTAAAACCAAAACACATGTCGTCATGATATCACAACATCA	ENSP00000265361.3:n.103+13745_103+13746insACTAACTAACATCAATGAT...
ENST00000411788.5:c.191+2895_191+2896insACTAACTAACATCAATGATTCATTTAAAACCAAAACACATGTCGTCATGATATCACAACATCA	ENSP00000395398.1:n.191+2895_191+2896insACTAACTAACATCAATGATTC...
ENST00000419255.6:c.103+13745_103+13746insACTAACTAACATCAATGATTCATTTAAAACCAAAACACATGTCGTCATGATATCACAACATCA	ENSP00000411193.2:n.103+13745_103+13746insACTAACTAACATCAATGAT...
ENST00000427167.5:c.191+2895_191+2896insACTAACTAACATCAATGATTCATTTAAAACCAAAACACATGTCGTCATGATATCACAACATCA	ENSP00000399891.1:n.191+2895_191+2896insACTAACTAACATCAATGATTC...
ENST00000458729.5:c.103+13745_103+13746insACTAACTAACATCAATGATTCATTTAAAACCAAAACACATGTCGTCATGATATCACAACATCA	ENSP00000393825.1:n.103+13745_103+13746insACTAACTAACATCAATGAT...
ENST00000487621.5:n.496+13745_496+13746insACTAACTAACATCAATGATTCATTTAAAACCAAAACACATGTCGTCATGATATCACAACATCA
NM_006379.3:c.103+13745_103+13746insACTAACTAACATCAATGATTCATTTAAAACCAAAACACATGTCGTCATGATATCACAACATCA	NP_006370.1:n.103+13745_103+13746insACTAACTAACATCAATGATTCATTT...
XM_005250113.1:c.-72+2895_-72+2896insACTAACTAACATCAATGATTCATTTAAAACCAAAACACATGTCGTCATGATATCACAACATCA	XP_005250170.1:n.-72+2895_-72+2896insACTAACTAACATCAATGATTCATT...
NM_001350120.1:c.157+13745_157+13746insACTAACTAACATCAATGATTCATTTAAAACCAAAACACATGTCGTCATGATATCACAACATCA	NP_001337049.1:n.157+13745_157+13746insACTAACTAACATCAATGATTCA...
NM_001350121.1:c.-72+2895_-72+2896insACTAACTAACATCAATGATTCATTTAAAACCAAAACACATGTCGTCATGATATCACAACATCA	NP_001337050.1:n.-72+2895_-72+2896insACTAACTAACATCAATGATTCATT...
NM_006379.4:c.103+13745_103+13746insACTAACTAACATCAATGATTCATTTAAAACCAAAACACATGTCGTCATGATATCACAACATCA	NP_006370.1:n.103+13745_103+13746insACTAACTAACATCAATGATTCATTT...
NM_006379.5:c.103+13745_103+13746insACTAACTAACATCAATGATTCATTTAAAACCAAAACACATGTCGTCATGATATCACAACATCA MANE Select	NP_006370.1:n.103+13745_103+13746insACTAACTAACATCAATGATTCATTT...
NM_001350120.2:c.157+13745_157+13746insACTAACTAACATCAATGATTCATTTAAAACCAAAACACATGTCGTCATGATATCACAACATCA	NP_001337049.1:n.157+13745_157+13746insACTAACTAACATCAATGATTCA...
NM_001350121.2:c.-72+2895_-72+2896insACTAACTAACATCAATGATTCATTTAAAACCAAAACACATGTCGTCATGATATCACAACATCA	NP_001337050.1:n.-72+2895_-72+2896insACTAACTAACATCAATGATTCATT...