Canonical Allele Identifier: CA1720489542

Gene: SEMA3C

Genomic Alleles

HGVS	Genome Assembly
NC_000007.14:g.80902950G= , CM000669.2:g.80902950G=	GRCh38
NC_000007.13:g.80532266G= , CM000669.1:g.80532266G=	GRCh37
NC_000007.12:g.80370202G=	NCBI36
NG_054744.1:g.24430C=

Transcript Alleles

HGVS	Amino-acid Change
ENST00000265361.8:c.103+13729C= MANE Select	ENSP00000265361.3:n.103+13729C=
ENST00000265361.7:c.103+13729C=	ENSP00000265361.3:n.103+13729C=
ENST00000411788.5:c.191+2879C=	ENSP00000395398.1:n.191+2879C=
ENST00000419255.6:c.103+13729C=	ENSP00000411193.2:n.103+13729C=
ENST00000427167.5:c.191+2879C=	ENSP00000399891.1:n.191+2879C=
ENST00000458729.5:c.103+13729C=	ENSP00000393825.1:n.103+13729C=
ENST00000487621.5:n.496+13729C=
NM_006379.3:c.103+13729C=	NP_006370.1:n.103+13729C=
XM_005250113.1:c.-72+2879C=	XP_005250170.1:n.-72+2879C=
NM_001350120.1:c.157+13729C=	NP_001337049.1:n.157+13729C=
NM_001350121.1:c.-72+2879C=	NP_001337050.1:n.-72+2879C=
NM_006379.4:c.103+13729C=	NP_006370.1:n.103+13729C=
NM_006379.5:c.103+13729C= MANE Select	NP_006370.1:n.103+13729C=
NM_001350120.2:c.157+13729C=	NP_001337049.1:n.157+13729C=
NM_001350121.2:c.-72+2879C=	NP_001337050.1:n.-72+2879C=