Canonical Allele Identifier: CA1721661763

Gene: SEMA3E

Genomic Alleles

HGVS	Genome Assembly
NC_000007.14:g.83392482_83392485delinsTTAA , CM000669.2:g.83392482_83392485delinsTTAA	GRCh38
NC_000007.13:g.83021798_83021801delinsTTAA , CM000669.1:g.83021798_83021801delinsTTAA	GRCh37
NC_000007.12:g.82859734_82859737delinsTTAA	NCBI36
NG_021242.1:g.261679_261682delinsTTAA
NG_021242.2:g.261679_261682delinsTTAA

Transcript Alleles

HGVS	Amino-acid Change
ENST00000427262.6:c.1487+70_1487+73delinsTTAA	ENSP00000405052.1:n.1487+70_1487+73delinsTTAA
ENST00000642232.1:c.1667+70_1667+73delinsTTAA	ENSP00000494064.1:n.1667+70_1667+73delinsTTAA
ENST00000643230.2:c.1667+70_1667+73delinsTTAA MANE Select	ENSP00000496491.1:n.1667+70_1667+73delinsTTAA
ENST00000643441.1:n.1652+70_1652+73delinsTTAA
ENST00000307792.7:c.1667+70_1667+73delinsTTAA	ENSP00000303212.3:n.1667+70_1667+73delinsTTAA
ENST00000427262.5:c.1487+70_1487+73delinsTTAA	ENSP00000405052.1:n.1487+70_1487+73delinsTTAA
NM_001178129.1:c.1487+70_1487+73delinsTTAA	NP_001171600.1:n.1487+70_1487+73delinsTTAA
NM_012431.2:c.1667+70_1667+73delinsTTAA	NP_036563.1:n.1667+70_1667+73delinsTTAA
XM_011516715.1:c.1667+70_1667+73delinsTTAA	XP_011515017.1:n.1667+70_1667+73delinsTTAA
NM_012431.3:c.1667+70_1667+73delinsTTAA MANE Select	NP_036563.1:n.1667+70_1667+73delinsTTAA
NM_001178129.2:c.1487+70_1487+73delinsTTAA	NP_001171600.1:n.1487+70_1487+73delinsTTAA