Canonical Allele Identifier: CA1720489551

Gene: SEMA3C

Genomic Alleles

HGVS	Genome Assembly
NC_000007.14:g.80902967_80902968delinsAT , CM000669.2:g.80902967_80902968delinsAT	GRCh38
NC_000007.13:g.80532283_80532284delinsAT , CM000669.1:g.80532283_80532284delinsAT	GRCh37
NC_000007.12:g.80370219_80370220delinsAT	NCBI36
NG_054744.1:g.24412_24413delinsAT

Transcript Alleles

HGVS	Amino-acid Change
ENST00000265361.8:c.103+13711_103+13712delinsAT MANE Select	ENSP00000265361.3:n.103+13711_103+13712delinsAT
ENST00000265361.7:c.103+13711_103+13712delinsAT	ENSP00000265361.3:n.103+13711_103+13712delinsAT
ENST00000411788.5:c.191+2861_191+2862delinsAT	ENSP00000395398.1:n.191+2861_191+2862delinsAT
ENST00000419255.6:c.103+13711_103+13712delinsAT	ENSP00000411193.2:n.103+13711_103+13712delinsAT
ENST00000427167.5:c.191+2861_191+2862delinsAT	ENSP00000399891.1:n.191+2861_191+2862delinsAT
ENST00000458729.5:c.103+13711_103+13712delinsAT	ENSP00000393825.1:n.103+13711_103+13712delinsAT
ENST00000487621.5:n.496+13711_496+13712delinsAT
NM_006379.3:c.103+13711_103+13712delinsAT	NP_006370.1:n.103+13711_103+13712delinsAT
XM_005250113.1:c.-72+2861_-72+2862delinsAT	XP_005250170.1:n.-72+2861_-72+2862delinsAT
NM_001350120.1:c.157+13711_157+13712delinsAT	NP_001337049.1:n.157+13711_157+13712delinsAT
NM_001350121.1:c.-72+2861_-72+2862delinsAT	NP_001337050.1:n.-72+2861_-72+2862delinsAT
NM_006379.4:c.103+13711_103+13712delinsAT	NP_006370.1:n.103+13711_103+13712delinsAT
NM_006379.5:c.103+13711_103+13712delinsAT MANE Select	NP_006370.1:n.103+13711_103+13712delinsAT
NM_001350120.2:c.157+13711_157+13712delinsAT	NP_001337049.1:n.157+13711_157+13712delinsAT
NM_001350121.2:c.-72+2861_-72+2862delinsAT	NP_001337050.1:n.-72+2861_-72+2862delinsAT