Canonical Allele Identifier: CA1721952981

Gene: SEMA3A

Genomic Alleles

HGVS	Genome Assembly
NC_000007.14:g.83981439G= , CM000669.2:g.83981439G=	GRCh38
NC_000007.13:g.83610755G= , CM000669.1:g.83610755G=	GRCh37
NC_000007.12:g.83448691G=	NCBI36
NG_011489.1:g.218463C=

Transcript Alleles

HGVS	Amino-acid Change
ENST00000265362.9:c.1534C= MANE Select	ENSP00000265362.3:p.Leu512=
ENST00000265362.8:c.1534C=	ENSP00000265362.3:p.Leu512=
ENST00000436949.5:c.1534C=	ENSP00000415260.1:p.Leu512=
NM_006080.2:c.1534C=	NP_006071.1:p.Leu512=
XM_005250110.2:c.1534C=	XP_005250167.1:p.Leu512=
XM_005250111.3:c.1534C=	XP_005250168.1:p.Leu512=
XM_006715839.2:c.1534C=	XP_006715902.1:p.Leu512=
XM_011515734.1:c.1534C=	XP_011514036.1:p.Leu512=
XM_011515735.1:c.1534C=	XP_011514037.1:p.Leu512=
XM_005250110.3:c.1534C=	XP_005250167.1:p.Leu512=
XM_005250111.4:c.1534C=	XP_005250168.1:p.Leu512=
XM_006715839.3:c.1534C=	XP_006715902.1:p.Leu512=
XM_011515734.3:c.1534C=	XP_011514036.1:p.Leu512=
XM_017011673.1:c.1534C=	XP_016867162.1:p.Leu512=
XM_024446633.1:c.1534C=	XP_024302401.1:p.Leu512=
NM_006080.3:c.1534C= MANE Select	NP_006071.1:p.Leu512=