Canonical Allele Identifier: CA1721974567

Gene: SEMA3A

Genomic Alleles

HGVS	Genome Assembly
NC_000007.14:g.84027432A= , CM000669.2:g.84027432A=	GRCh38
NC_000007.13:g.83656748A= , CM000669.1:g.83656748A=	GRCh37
NC_000007.12:g.83494684A=	NCBI36
NG_011489.1:g.172470T=

Transcript Alleles

HGVS	Amino-acid change
ENST00000265362.9:c.668-13081T= MANE Select	ENSP00000265362.3:n.668-13081T=
ENST00000265362.8:c.668-13081T=	ENSP00000265362.3:n.668-13081T=
ENST00000436949.5:c.668-13081T=	ENSP00000415260.1:n.668-13081T=
NM_006080.2:c.668-13081T=	NP_006071.1:n.668-13081T=
XM_005250110.2:c.668-13081T=	XP_005250167.1:n.668-13081T=
XM_005250111.3:c.668-13081T=	XP_005250168.1:n.668-13081T=
XM_006715839.2:c.668-13081T=	XP_006715902.1:n.668-13081T=
XM_011515734.1:c.668-13081T=	XP_011514036.1:n.668-13081T=
XM_011515735.1:c.668-13081T=	XP_011514037.1:n.668-13081T=
XM_005250110.3:c.668-13081T=	XP_005250167.1:n.668-13081T=
XM_005250111.4:c.668-13081T=	XP_005250168.1:n.668-13081T=
XM_006715839.3:c.668-13081T=	XP_006715902.1:n.668-13081T=
XM_011515734.3:c.668-13081T=	XP_011514036.1:n.668-13081T=
XM_017011673.1:c.668-13081T=	XP_016867162.1:n.668-13081T=
XM_024446633.1:c.668-13081T=	XP_024302401.1:n.668-13081T=
NM_006080.3:c.668-13081T= MANE Select	NP_006071.1:n.668-13081T=