Canonical Allele Identifier: CA918061622

Gene: SEMA3E

Linked Data

• dbSNP Id: rs1562760028

Genomic Alleles

HGVS	Genome Assembly
NC_000007.14:g.83392483_83392486del , CM000669.2:g.83392483_83392486del	GRCh38
NC_000007.13:g.83021799_83021802del , CM000669.1:g.83021799_83021802del	GRCh37
NC_000007.12:g.82859735_82859738del	NCBI36
NG_021242.1:g.261678_261681del
NG_021242.2:g.261678_261681del

Transcript Alleles

HGVS	Amino-acid Change
ENST00000427262.6:c.1487+69_1487+72del	ENSP00000405052.1:n.1487+69_1487+72del
ENST00000642232.1:c.1667+69_1667+72del	ENSP00000494064.1:n.1667+69_1667+72del
ENST00000643230.2:c.1667+69_1667+72del MANE Select	ENSP00000496491.1:n.1667+69_1667+72del
ENST00000643441.1:n.1652+69_1652+72del
ENST00000307792.7:c.1667+69_1667+72del	ENSP00000303212.3:n.1667+69_1667+72del
ENST00000427262.5:c.1487+69_1487+72del	ENSP00000405052.1:n.1487+69_1487+72del
NM_001178129.1:c.1487+69_1487+72del	NP_001171600.1:n.1487+69_1487+72del
NM_012431.2:c.1667+69_1667+72del	NP_036563.1:n.1667+69_1667+72del
XM_011516715.1:c.1667+69_1667+72del	XP_011515017.1:n.1667+69_1667+72del
NM_012431.3:c.1667+69_1667+72del MANE Select	NP_036563.1:n.1667+69_1667+72del
NM_001178129.2:c.1487+69_1487+72del	NP_001171600.1:n.1487+69_1487+72del