Canonical Allele Identifier: CA1721952690

Gene: SEMA3A

Genomic Alleles

HGVS	Genome Assembly
NC_000007.14:g.83981130_83981131delinsCT , CM000669.2:g.83981130_83981131delinsCT	GRCh38
NC_000007.13:g.83610446_83610447delinsCT , CM000669.1:g.83610446_83610447delinsCT	GRCh37
NC_000007.12:g.83448382_83448383delinsCT	NCBI36
NG_011489.1:g.218771_218772delinsAG

Transcript Alleles

HGVS	Amino-acid Change
ENST00000265362.9:c.1652+190_1652+191delinsAG MANE Select	ENSP00000265362.3:n.1652+190_1652+191delinsAG
ENST00000265362.8:c.1652+190_1652+191delinsAG	ENSP00000265362.3:n.1652+190_1652+191delinsAG
ENST00000436949.5:c.1652+190_1652+191delinsAG	ENSP00000415260.1:n.1652+190_1652+191delinsAG
NM_006080.2:c.1652+190_1652+191delinsAG	NP_006071.1:n.1652+190_1652+191delinsAG
XM_005250110.2:c.1652+190_1652+191delinsAG	XP_005250167.1:n.1652+190_1652+191delinsAG
XM_005250111.3:c.1652+190_1652+191delinsAG	XP_005250168.1:n.1652+190_1652+191delinsAG
XM_006715839.2:c.1652+190_1652+191delinsAG	XP_006715902.1:n.1652+190_1652+191delinsAG
XM_011515734.1:c.1652+190_1652+191delinsAG	XP_011514036.1:n.1652+190_1652+191delinsAG
XM_011515735.1:c.1652+190_1652+191delinsAG	XP_011514037.1:n.1652+190_1652+191delinsAG
XM_005250110.3:c.1652+190_1652+191delinsAG	XP_005250167.1:n.1652+190_1652+191delinsAG
XM_005250111.4:c.1652+190_1652+191delinsAG	XP_005250168.1:n.1652+190_1652+191delinsAG
XM_006715839.3:c.1652+190_1652+191delinsAG	XP_006715902.1:n.1652+190_1652+191delinsAG
XM_011515734.3:c.1652+190_1652+191delinsAG	XP_011514036.1:n.1652+190_1652+191delinsAG
XM_017011673.1:c.1652+190_1652+191delinsAG	XP_016867162.1:n.1652+190_1652+191delinsAG
XM_024446633.1:c.1652+190_1652+191delinsAG	XP_024302401.1:n.1652+190_1652+191delinsAG
NM_006080.3:c.1652+190_1652+191delinsAG MANE Select	NP_006071.1:n.1652+190_1652+191delinsAG