Canonical Allele Identifier: CA1721953106

Gene: SEMA3A

Genomic Alleles

HGVS	Genome Assembly
NC_000007.14:g.83981545_83981547delinsAAG , CM000669.2:g.83981545_83981547delinsAAG	GRCh38
NC_000007.13:g.83610861_83610863delinsAAG , CM000669.1:g.83610861_83610863delinsAAG	GRCh37
NC_000007.12:g.83448797_83448799delinsAAG	NCBI36
NG_011489.1:g.218355_218357delinsCTT

Transcript Alleles

HGVS	Amino-acid Change
ENST00000265362.9:c.1495-69_1495-67delinsCTT MANE Select	ENSP00000265362.3:n.1495-69_1495-67delinsCTT
ENST00000265362.8:c.1495-69_1495-67delinsCTT	ENSP00000265362.3:n.1495-69_1495-67delinsCTT
ENST00000436949.5:c.1495-69_1495-67delinsCTT	ENSP00000415260.1:n.1495-69_1495-67delinsCTT
NM_006080.2:c.1495-69_1495-67delinsCTT	NP_006071.1:n.1495-69_1495-67delinsCTT
XM_005250110.2:c.1495-69_1495-67delinsCTT	XP_005250167.1:n.1495-69_1495-67delinsCTT
XM_005250111.3:c.1495-69_1495-67delinsCTT	XP_005250168.1:n.1495-69_1495-67delinsCTT
XM_006715839.2:c.1495-69_1495-67delinsCTT	XP_006715902.1:n.1495-69_1495-67delinsCTT
XM_011515734.1:c.1495-69_1495-67delinsCTT	XP_011514036.1:n.1495-69_1495-67delinsCTT
XM_011515735.1:c.1495-69_1495-67delinsCTT	XP_011514037.1:n.1495-69_1495-67delinsCTT
XM_005250110.3:c.1495-69_1495-67delinsCTT	XP_005250167.1:n.1495-69_1495-67delinsCTT
XM_005250111.4:c.1495-69_1495-67delinsCTT	XP_005250168.1:n.1495-69_1495-67delinsCTT
XM_006715839.3:c.1495-69_1495-67delinsCTT	XP_006715902.1:n.1495-69_1495-67delinsCTT
XM_011515734.3:c.1495-69_1495-67delinsCTT	XP_011514036.1:n.1495-69_1495-67delinsCTT
XM_017011673.1:c.1495-69_1495-67delinsCTT	XP_016867162.1:n.1495-69_1495-67delinsCTT
XM_024446633.1:c.1495-69_1495-67delinsCTT	XP_024302401.1:n.1495-69_1495-67delinsCTT
NM_006080.3:c.1495-69_1495-67delinsCTT MANE Select	NP_006071.1:n.1495-69_1495-67delinsCTT