Canonical Allele Identifier: CA1363819868

Gene: SEMA3F

Genomic Alleles

HGVS	Genome Assembly
NC_000003.12:g.50159131G= , CM000665.2:g.50159131G=	GRCh38
NC_000003.11:g.50196564G= , CM000665.1:g.50196564G=	GRCh37
NC_000003.10:g.50171568G=	NCBI36

Transcript Alleles

HGVS	Amino-acid change
ENST00000002829.8:c.-48-444G= MANE Select	ENSP00000002829.3:n.-48-444G=
ENST00000002829.7:c.-48-444G=	ENSP00000002829.3:n.-48-444G=
ENST00000413852.5:c.-135-561G=	ENSP00000388931.1:n.-135-561G=
ENST00000414301.5:c.-40-452G=	ENSP00000392588.1:n.-40-452G=
ENST00000426511.5:c.-48-444G=	ENSP00000400549.1:n.-48-444G=
ENST00000434342.5:c.-206G=	ENSP00000409859.1:n.-206G=
ENST00000450338.5:c.-48-444G=	ENSP00000398399.1:n.-48-444G=
NM_004186.3:c.-48-444G=	NP_004177.3:n.-48-444G=
XM_005265381.3:c.-48-444G=	XP_005265438.1:n.-48-444G=
XM_005265382.3:c.-48-444G=	XP_005265439.1:n.-48-444G=
XM_006713290.2:c.-48-444G=	XP_006713353.1:n.-48-444G=
XM_011533998.1:c.-48-444G=	XP_011532300.1:n.-48-444G=
XM_011533999.1:c.-206G=	XP_011532301.1:n.-206G=
XM_011534000.1:c.-48-444G=	XP_011532302.1:n.-48-444G=
XR_940487.1:n.150-444G=
NM_001318798.1:c.-135-561G=	NP_001305727.1:n.-135-561G=
NM_001318800.1:c.-206G=	NP_001305729.1:n.-206G=
NM_004186.4:c.-48-444G=	NP_004177.3:n.-48-444G=
XM_005265381.4:c.-48-444G=	XP_005265438.1:n.-48-444G=
XM_005265382.4:c.-48-444G=	XP_005265439.1:n.-48-444G=
XM_006713290.3:c.-48-444G=	XP_006713353.1:n.-48-444G=
XM_011533998.2:c.-48-444G=	XP_011532300.1:n.-48-444G=
XM_011534000.2:c.-48-444G=	XP_011532302.1:n.-48-444G=
XR_940487.2:n.88-444G=
NM_004186.5:c.-48-444G= MANE Select	NP_004177.3:n.-48-444G=
NM_001318798.2:c.-135-561G=	NP_001305727.1:n.-135-561G=
NM_001318800.2:c.-206G=	NP_001305729.1:n.-206G=