Canonical Allele Identifier: CA1721661764

Gene: SEMA3E

Genomic Alleles

HGVS	Genome Assembly
NC_000007.14:g.83392482_83392486delinsTTAAA , CM000669.2:g.83392482_83392486delinsTTAAA	GRCh38
NC_000007.13:g.83021798_83021802delinsTTAAA , CM000669.1:g.83021798_83021802delinsTTAAA	GRCh37
NC_000007.12:g.82859734_82859738delinsTTAAA	NCBI36
NG_021242.1:g.261678_261682delinsTTTAA
NG_021242.2:g.261678_261682delinsTTTAA

Transcript Alleles

HGVS	Amino-acid Change
ENST00000427262.6:c.1487+69_1487+73delinsTTTAA	ENSP00000405052.1:n.1487+69_1487+73delinsTTTAA
ENST00000642232.1:c.1667+69_1667+73delinsTTTAA	ENSP00000494064.1:n.1667+69_1667+73delinsTTTAA
ENST00000643230.2:c.1667+69_1667+73delinsTTTAA MANE Select	ENSP00000496491.1:n.1667+69_1667+73delinsTTTAA
ENST00000643441.1:n.1652+69_1652+73delinsTTTAA
ENST00000307792.7:c.1667+69_1667+73delinsTTTAA	ENSP00000303212.3:n.1667+69_1667+73delinsTTTAA
ENST00000427262.5:c.1487+69_1487+73delinsTTTAA	ENSP00000405052.1:n.1487+69_1487+73delinsTTTAA
NM_001178129.1:c.1487+69_1487+73delinsTTTAA	NP_001171600.1:n.1487+69_1487+73delinsTTTAA
NM_012431.2:c.1667+69_1667+73delinsTTTAA	NP_036563.1:n.1667+69_1667+73delinsTTTAA
XM_011516715.1:c.1667+69_1667+73delinsTTTAA	XP_011515017.1:n.1667+69_1667+73delinsTTTAA
NM_012431.3:c.1667+69_1667+73delinsTTTAA MANE Select	NP_036563.1:n.1667+69_1667+73delinsTTTAA
NM_001178129.2:c.1487+69_1487+73delinsTTTAA	NP_001171600.1:n.1487+69_1487+73delinsTTTAA