Canonical Allele Identifier: CA2578926469

Gene: SEMA3E

Genomic Alleles

HGVS	Genome Assembly
NC_000007.14:g.83392734_83392735del , CM000669.2:g.83392734_83392735del	GRCh38
NC_000007.13:g.83022050_83022051del , CM000669.1:g.83022050_83022051del	GRCh37
NC_000007.12:g.82859986_82859987del	NCBI36
NG_021242.1:g.261430_261431del
NG_021242.2:g.261430_261431del

Transcript Alleles

HGVS	Amino-acid change
ENST00000427262.6:c.1321-13_1321-12del	ENSP00000405052.1:n.1321-13_1321-12del
ENST00000642232.1:c.1501-13_1501-12del	ENSP00000494064.1:n.1501-13_1501-12del
ENST00000643230.2:c.1501-13_1501-12del MANE Select	ENSP00000496491.1:n.1501-13_1501-12del
ENST00000643441.1:n.1486-13_1486-12del
ENST00000307792.7:c.1501-13_1501-12del	ENSP00000303212.3:n.1501-13_1501-12del
ENST00000427262.5:c.1321-13_1321-12del	ENSP00000405052.1:n.1321-13_1321-12del
NM_001178129.1:c.1321-13_1321-12del	NP_001171600.1:n.1321-13_1321-12del
NM_012431.2:c.1501-13_1501-12del	NP_036563.1:n.1501-13_1501-12del
XM_011516715.1:c.1501-13_1501-12del	XP_011515017.1:n.1501-13_1501-12del
NM_012431.3:c.1501-13_1501-12del MANE Select	NP_036563.1:n.1501-13_1501-12del
NM_001178129.2:c.1321-13_1321-12del	NP_001171600.1:n.1321-13_1321-12del