Canonical Allele Identifier: CA3148767702

Gene: SEMA3A

Genomic Alleles

HGVS	Genome Assembly
NC_000007.14:g.83961440G= , CM000669.2:g.83961440G=	GRCh38
NC_000007.13:g.83590756G= , CM000669.1:g.83590756G=	GRCh37
NC_000007.12:g.83428692G=	NCBI36
NG_011489.1:g.238462C=

Transcript Alleles

HGVS	Amino-acid Change
NM_006080.3:c.2247C= MANE Select	NP_006071.1:p.His749=
ENST00000265362.9:c.2247C= MANE Select	ENSP00000265362.3:p.His749=
NM_006080.2:c.2247C=	NP_006071.1:p.His749=
ENST00000265362.8:c.2247C=	ENSP00000265362.3:p.His749=
ENST00000436949.5:c.2247C=	ENSP00000415260.1:p.His749=
XM_005250110.2:c.2247C=	XP_005250167.1:p.His749=
XM_005250110.3:c.2247C=	XP_005250167.1:p.His749=
XM_005250111.3:c.2247C=	XP_005250168.1:p.His749=
XM_005250111.4:c.2247C=	XP_005250168.1:p.His749=
XM_006715839.2:c.2247C=	XP_006715902.1:p.His749=
XM_006715839.3:c.2247C=	XP_006715902.1:p.His749=
XM_011515734.1:c.2247C=	XP_011514036.1:p.His749=
XM_011515734.3:c.2247C=	XP_011514036.1:p.His749=
XM_017011673.1:c.2247C=	XP_016867162.1:p.His749=
XM_024446633.1:c.2247C=	XP_024302401.1:p.His749=