Canonical Allele Identifier: CA1721661903

Gene: SEMA3E

Genomic Alleles

HGVS	Genome Assembly
NC_000007.14:g.83392555_83392556delinsCT , CM000669.2:g.83392555_83392556delinsCT	GRCh38
NC_000007.13:g.83021871_83021872delinsCT , CM000669.1:g.83021871_83021872delinsCT	GRCh37
NC_000007.12:g.82859807_82859808delinsCT	NCBI36
NG_021242.1:g.261608_261609delinsAG
NG_021242.2:g.261608_261609delinsAG

Transcript Alleles

HGVS	Amino-acid Change
ENST00000427262.6:c.1486_1487delinsAG	ENSP00000405052.1:p.Arg496=
ENST00000642232.1:c.1666_1667delinsAG	ENSP00000494064.1:p.Arg556=
ENST00000643230.2:c.1666_1667delinsAG MANE Select	ENSP00000496491.1:p.Arg556=
ENST00000643441.1:n.1651_1652delinsAG
ENST00000307792.7:c.1666_1667delinsAG	ENSP00000303212.3:p.Arg556=
ENST00000427262.5:c.1486_1487delinsAG	ENSP00000405052.1:p.Arg496=
NM_001178129.1:c.1486_1487delinsAG	NP_001171600.1:p.Arg496=
NM_012431.2:c.1666_1667delinsAG	NP_036563.1:p.Arg556=
XM_011516715.1:c.1666_1667delinsAG	XP_011515017.1:p.Arg556=
NM_012431.3:c.1666_1667delinsAG MANE Select	NP_036563.1:p.Arg556=
NM_001178129.2:c.1486_1487delinsAG	NP_001171600.1:p.Arg496=