Canonical Allele Identifier: CA1720489418
Gene: SEMA3C HGNC NCBI

Genomic Alleles

HGVS Genome Assembly
NC_000007.14:g.80902713G= , CM000669.2:g.80902713G= GRCh38
NC_000007.13:g.80532029G= , CM000669.1:g.80532029G= GRCh37
NC_000007.12:g.80369965G= NCBI36
NG_054744.1:g.24667C=

Transcript Alleles

HGVS Amino-acid change
ENST00000265361.8:c.103+13966C= MANE Select ENSP00000265361.3:n.103+13966C=
ENST00000265361.7:c.103+13966C= ENSP00000265361.3:n.103+13966C=
ENST00000411788.5:c.191+3116C= ENSP00000395398.1:n.191+3116C=
ENST00000419255.6:c.103+13966C= ENSP00000411193.2:n.103+13966C=
ENST00000427167.5:c.191+3116C= ENSP00000399891.1:n.191+3116C=
ENST00000458729.5:c.103+13966C= ENSP00000393825.1:n.103+13966C=
ENST00000487621.5:n.496+13966C=
NM_006379.3:c.103+13966C= NP_006370.1:n.103+13966C=
XM_005250113.1:c.-72+3116C= XP_005250170.1:n.-72+3116C=
NM_001350120.1:c.157+13966C= NP_001337049.1:n.157+13966C=
NM_001350121.1:c.-72+3116C= NP_001337050.1:n.-72+3116C=
NM_006379.4:c.103+13966C= NP_006370.1:n.103+13966C=
NM_006379.5:c.103+13966C= MANE Select NP_006370.1:n.103+13966C=
NM_001350120.2:c.157+13966C= NP_001337049.1:n.157+13966C=
NM_001350121.2:c.-72+3116C= NP_001337050.1:n.-72+3116C=