Canonical Allele Identifier: CA2683561521

Gene: SEMA3A

Linked Data

• gnomAD v4: 7-83981489-A-C

Genomic Alleles

HGVS	Genome Assembly
NC_000007.14:g.83981489A>C , CM000669.2:g.83981489A>C	GRCh38
NC_000007.13:g.83610805A>C , CM000669.1:g.83610805A>C	GRCh37
NC_000007.12:g.83448741A>C	NCBI36
NG_011489.1:g.218413T>G

Transcript Alleles

HGVS	Amino-acid Change
ENST00000265362.9:c.1495-11T>G MANE Select	ENSP00000265362.3:n.1495-11T>G
ENST00000265362.8:c.1495-11T>G	ENSP00000265362.3:n.1495-11T>G
ENST00000436949.5:c.1495-11T>G	ENSP00000415260.1:n.1495-11T>G
NM_006080.2:c.1495-11T>G	NP_006071.1:n.1495-11T>G
XM_005250110.2:c.1495-11T>G	XP_005250167.1:n.1495-11T>G
XM_005250111.3:c.1495-11T>G	XP_005250168.1:n.1495-11T>G
XM_006715839.2:c.1495-11T>G	XP_006715902.1:n.1495-11T>G
XM_011515734.1:c.1495-11T>G	XP_011514036.1:n.1495-11T>G
XM_011515735.1:c.1495-11T>G	XP_011514037.1:n.1495-11T>G
XM_005250110.3:c.1495-11T>G	XP_005250167.1:n.1495-11T>G
XM_005250111.4:c.1495-11T>G	XP_005250168.1:n.1495-11T>G
XM_006715839.3:c.1495-11T>G	XP_006715902.1:n.1495-11T>G
XM_011515734.3:c.1495-11T>G	XP_011514036.1:n.1495-11T>G
XM_017011673.1:c.1495-11T>G	XP_016867162.1:n.1495-11T>G
XM_024446633.1:c.1495-11T>G	XP_024302401.1:n.1495-11T>G
NM_006080.3:c.1495-11T>G MANE Select	NP_006071.1:n.1495-11T>G