Canonical Allele Identifier: CA2665807302

Gene: SEMA3F

Linked Data

• gnomAD v4: 3-50159016-T-C

Genomic Alleles

HGVS	Genome Assembly
NC_000003.12:g.50159016T>C , CM000665.2:g.50159016T>C	GRCh38
NC_000003.11:g.50196449T>C , CM000665.1:g.50196449T>C	GRCh37
NC_000003.10:g.50171453T>C	NCBI36

Transcript Alleles

HGVS	Amino-acid Change
ENST00000002829.8:c.-48-559T>C MANE Select	ENSP00000002829.3:n.-48-559T>C
ENST00000002829.7:c.-48-559T>C	ENSP00000002829.3:n.-48-559T>C
ENST00000413852.5:c.-135-676T>C	ENSP00000388931.1:n.-135-676T>C
ENST00000414301.5:c.-40-567T>C	ENSP00000392588.1:n.-40-567T>C
ENST00000426511.5:c.-48-559T>C	ENSP00000400549.1:n.-48-559T>C
ENST00000450338.5:c.-48-559T>C	ENSP00000398399.1:n.-48-559T>C
NM_004186.3:c.-48-559T>C	NP_004177.3:n.-48-559T>C
XM_005265381.3:c.-48-559T>C	XP_005265438.1:n.-48-559T>C
XM_005265382.3:c.-48-559T>C	XP_005265439.1:n.-48-559T>C
XM_006713290.2:c.-48-559T>C	XP_006713353.1:n.-48-559T>C
XM_011533998.1:c.-48-559T>C	XP_011532300.1:n.-48-559T>C
XM_011534000.1:c.-48-559T>C	XP_011532302.1:n.-48-559T>C
XR_940487.1:n.150-559T>C
NM_001318798.1:c.-135-676T>C	NP_001305727.1:n.-135-676T>C
NM_004186.4:c.-48-559T>C	NP_004177.3:n.-48-559T>C
XM_005265381.4:c.-48-559T>C	XP_005265438.1:n.-48-559T>C
XM_005265382.4:c.-48-559T>C	XP_005265439.1:n.-48-559T>C
XM_006713290.3:c.-48-559T>C	XP_006713353.1:n.-48-559T>C
XM_011533998.2:c.-48-559T>C	XP_011532300.1:n.-48-559T>C
XM_011534000.2:c.-48-559T>C	XP_011532302.1:n.-48-559T>C
XR_940487.2:n.88-559T>C
NM_004186.5:c.-48-559T>C MANE Select	NP_004177.3:n.-48-559T>C
NM_001318798.2:c.-135-676T>C	NP_001305727.1:n.-135-676T>C