Canonical Allele Identifier: CA1103891540
Gene: SEMA3A HGNC NCBI

Linked Data

dbSNP Id: rs1789418191

Genomic Alleles

HGVS Genome Assembly
NC_000007.14:g.83981548_83981549del , CM000669.2:g.83981548_83981549del GRCh38
NC_000007.13:g.83610864_83610865del , CM000669.1:g.83610864_83610865del GRCh37
NC_000007.12:g.83448800_83448801del NCBI36
NG_011489.1:g.218355_218356del

Transcript Alleles

HGVS Amino-acid Change
ENST00000265362.9:c.1495-69_1495-68del MANE Select ENSP00000265362.3:n.1495-69_1495-68del
ENST00000265362.8:c.1495-69_1495-68del ENSP00000265362.3:n.1495-69_1495-68del
ENST00000436949.5:c.1495-69_1495-68del ENSP00000415260.1:n.1495-69_1495-68del
NM_006080.2:c.1495-69_1495-68del NP_006071.1:n.1495-69_1495-68del
XM_005250110.2:c.1495-69_1495-68del XP_005250167.1:n.1495-69_1495-68del
XM_005250111.3:c.1495-69_1495-68del XP_005250168.1:n.1495-69_1495-68del
XM_006715839.2:c.1495-69_1495-68del XP_006715902.1:n.1495-69_1495-68del
XM_011515734.1:c.1495-69_1495-68del XP_011514036.1:n.1495-69_1495-68del
XM_011515735.1:c.1495-69_1495-68del XP_011514037.1:n.1495-69_1495-68del
XM_005250110.3:c.1495-69_1495-68del XP_005250167.1:n.1495-69_1495-68del
XM_005250111.4:c.1495-69_1495-68del XP_005250168.1:n.1495-69_1495-68del
XM_006715839.3:c.1495-69_1495-68del XP_006715902.1:n.1495-69_1495-68del
XM_011515734.3:c.1495-69_1495-68del XP_011514036.1:n.1495-69_1495-68del
XM_017011673.1:c.1495-69_1495-68del XP_016867162.1:n.1495-69_1495-68del
XM_024446633.1:c.1495-69_1495-68del XP_024302401.1:n.1495-69_1495-68del
NM_006080.3:c.1495-69_1495-68del MANE Select NP_006071.1:n.1495-69_1495-68del