Canonical Allele Identifier: CA1720489518

Gene: SEMA3C

Genomic Alleles

HGVS	Genome Assembly
NC_000007.14:g.80902914_80902915delinsAC , CM000669.2:g.80902914_80902915delinsAC	GRCh38
NC_000007.13:g.80532230_80532231delinsAC , CM000669.1:g.80532230_80532231delinsAC	GRCh37
NC_000007.12:g.80370166_80370167delinsAC	NCBI36
NG_054744.1:g.24465_24466delinsGT

Transcript Alleles

HGVS	Amino-acid Change
ENST00000265361.8:c.103+13764_103+13765delinsGT MANE Select	ENSP00000265361.3:n.103+13764_103+13765delinsGT
ENST00000265361.7:c.103+13764_103+13765delinsGT	ENSP00000265361.3:n.103+13764_103+13765delinsGT
ENST00000411788.5:c.191+2914_191+2915delinsGT	ENSP00000395398.1:n.191+2914_191+2915delinsGT
ENST00000419255.6:c.103+13764_103+13765delinsGT	ENSP00000411193.2:n.103+13764_103+13765delinsGT
ENST00000427167.5:c.191+2914_191+2915delinsGT	ENSP00000399891.1:n.191+2914_191+2915delinsGT
ENST00000458729.5:c.103+13764_103+13765delinsGT	ENSP00000393825.1:n.103+13764_103+13765delinsGT
ENST00000487621.5:n.496+13764_496+13765delinsGT
NM_006379.3:c.103+13764_103+13765delinsGT	NP_006370.1:n.103+13764_103+13765delinsGT
XM_005250113.1:c.-72+2914_-72+2915delinsGT	XP_005250170.1:n.-72+2914_-72+2915delinsGT
NM_001350120.1:c.157+13764_157+13765delinsGT	NP_001337049.1:n.157+13764_157+13765delinsGT
NM_001350121.1:c.-72+2914_-72+2915delinsGT	NP_001337050.1:n.-72+2914_-72+2915delinsGT
NM_006379.4:c.103+13764_103+13765delinsGT	NP_006370.1:n.103+13764_103+13765delinsGT
NM_006379.5:c.103+13764_103+13765delinsGT MANE Select	NP_006370.1:n.103+13764_103+13765delinsGT
NM_001350120.2:c.157+13764_157+13765delinsGT	NP_001337049.1:n.157+13764_157+13765delinsGT
NM_001350121.2:c.-72+2914_-72+2915delinsGT	NP_001337050.1:n.-72+2914_-72+2915delinsGT