Canonical Allele Identifier: CA1722034259

Gene: SEMA3A

Genomic Alleles

HGVS	Genome Assembly
NC_000007.14:g.84143117_84143120delinsATCT , CM000669.2:g.84143117_84143120delinsATCT	GRCh38
NC_000007.13:g.83772433_83772436delinsATCT , CM000669.1:g.83772433_83772436delinsATCT	GRCh37
NC_000007.12:g.83610369_83610372delinsATCT	NCBI36
NG_011489.1:g.56782_56785delinsAGAT

Transcript Alleles

HGVS	Amino-acid Change
ENST00000265362.9:c.113-8169_113-8166delinsAGAT MANE Select	ENSP00000265362.3:n.113-8169_113-8166delinsAGAT
ENST00000265362.8:c.113-8169_113-8166delinsAGAT	ENSP00000265362.3:n.113-8169_113-8166delinsAGAT
ENST00000420047.1:c.113-8169_113-8166delinsAGAT	ENSP00000391900.1:n.113-8169_113-8166delinsAGAT
ENST00000436949.5:c.113-8169_113-8166delinsAGAT	ENSP00000415260.1:n.113-8169_113-8166delinsAGAT
NM_006080.2:c.113-8169_113-8166delinsAGAT	NP_006071.1:n.113-8169_113-8166delinsAGAT
XM_005250110.2:c.113-8169_113-8166delinsAGAT	XP_005250167.1:n.113-8169_113-8166delinsAGAT
XM_005250111.3:c.113-8169_113-8166delinsAGAT	XP_005250168.1:n.113-8169_113-8166delinsAGAT
XM_006715839.2:c.113-8169_113-8166delinsAGAT	XP_006715902.1:n.113-8169_113-8166delinsAGAT
XM_011515734.1:c.113-8169_113-8166delinsAGAT	XP_011514036.1:n.113-8169_113-8166delinsAGAT
XM_011515735.1:c.113-8169_113-8166delinsAGAT	XP_011514037.1:n.113-8169_113-8166delinsAGAT
XM_005250110.3:c.113-8169_113-8166delinsAGAT	XP_005250167.1:n.113-8169_113-8166delinsAGAT
XM_005250111.4:c.113-8169_113-8166delinsAGAT	XP_005250168.1:n.113-8169_113-8166delinsAGAT
XM_006715839.3:c.113-8169_113-8166delinsAGAT	XP_006715902.1:n.113-8169_113-8166delinsAGAT
XM_011515734.3:c.113-8169_113-8166delinsAGAT	XP_011514036.1:n.113-8169_113-8166delinsAGAT
XM_017011673.1:c.113-8169_113-8166delinsAGAT	XP_016867162.1:n.113-8169_113-8166delinsAGAT
XM_024446633.1:c.113-8169_113-8166delinsAGAT	XP_024302401.1:n.113-8169_113-8166delinsAGAT
NM_006080.3:c.113-8169_113-8166delinsAGAT MANE Select	NP_006071.1:n.113-8169_113-8166delinsAGAT