Canonical Allele Identifier: CA1721661771

Gene: SEMA3E

Genomic Alleles

HGVS	Genome Assembly
NC_000007.14:g.83392483_83392490delinsTAAAAAAA , CM000669.2:g.83392483_83392490delinsTAAAAAAA	GRCh38
NC_000007.13:g.83021799_83021806delinsTAAAAAAA , CM000669.1:g.83021799_83021806delinsTAAAAAAA	GRCh37
NC_000007.12:g.82859735_82859742delinsTAAAAAAA	NCBI36
NG_021242.1:g.261674_261681delinsTTTTTTTA
NG_021242.2:g.261674_261681delinsTTTTTTTA

Transcript Alleles

HGVS	Amino-acid Change
ENST00000427262.6:c.1487+65_1487+72delinsTTTTTTTA	ENSP00000405052.1:n.1487+65_1487+72delinsTTTTTTTA
ENST00000642232.1:c.1667+65_1667+72delinsTTTTTTTA	ENSP00000494064.1:n.1667+65_1667+72delinsTTTTTTTA
ENST00000643230.2:c.1667+65_1667+72delinsTTTTTTTA MANE Select	ENSP00000496491.1:n.1667+65_1667+72delinsTTTTTTTA
ENST00000643441.1:n.1652+65_1652+72delinsTTTTTTTA
ENST00000307792.7:c.1667+65_1667+72delinsTTTTTTTA	ENSP00000303212.3:n.1667+65_1667+72delinsTTTTTTTA
ENST00000427262.5:c.1487+65_1487+72delinsTTTTTTTA	ENSP00000405052.1:n.1487+65_1487+72delinsTTTTTTTA
NM_001178129.1:c.1487+65_1487+72delinsTTTTTTTA	NP_001171600.1:n.1487+65_1487+72delinsTTTTTTTA
NM_012431.2:c.1667+65_1667+72delinsTTTTTTTA	NP_036563.1:n.1667+65_1667+72delinsTTTTTTTA
XM_011516715.1:c.1667+65_1667+72delinsTTTTTTTA	XP_011515017.1:n.1667+65_1667+72delinsTTTTTTTA
NM_012431.3:c.1667+65_1667+72delinsTTTTTTTA MANE Select	NP_036563.1:n.1667+65_1667+72delinsTTTTTTTA
NM_001178129.2:c.1487+65_1487+72delinsTTTTTTTA	NP_001171600.1:n.1487+65_1487+72delinsTTTTTTTA