Canonical Allele Identifier: CA1721661912

Gene: SEMA3E

Genomic Alleles

HGVS	Genome Assembly
NC_000007.14:g.83392563A= , CM000669.2:g.83392563A=	GRCh38
NC_000007.13:g.83021879A= , CM000669.1:g.83021879A=	GRCh37
NC_000007.12:g.82859815A=	NCBI36
NG_021242.1:g.261601T=
NG_021242.2:g.261601T=

Transcript Alleles

HGVS	Amino-acid Change
ENST00000427262.6:c.1479T=	ENSP00000405052.1:p.His493=
ENST00000642232.1:c.1659T=	ENSP00000494064.1:p.His553=
ENST00000643230.2:c.1659T= MANE Select	ENSP00000496491.1:p.His553=
ENST00000643441.1:n.1644T=
ENST00000307792.7:c.1659T=	ENSP00000303212.3:p.His553=
ENST00000427262.5:c.1479T=	ENSP00000405052.1:p.His493=
NM_001178129.1:c.1479T=	NP_001171600.1:p.His493=
NM_012431.2:c.1659T=	NP_036563.1:p.His553=
XM_011516715.1:c.1659T=	XP_011515017.1:p.His553=
NM_012431.3:c.1659T= MANE Select	NP_036563.1:p.His553=
NM_001178129.2:c.1479T=	NP_001171600.1:p.His493=