Canonical Allele Identifier: CA1103931881
Gene: SEMA3A HGNC NCBI

Linked Data

dbSNP Id: rs1796345414

Genomic Alleles

HGVS Genome Assembly
NC_000007.14:g.84143113_84143114del , CM000669.2:g.84143113_84143114del GRCh38
NC_000007.13:g.83772429_83772430del , CM000669.1:g.83772429_83772430del GRCh37
NC_000007.12:g.83610365_83610366del NCBI36
NG_011489.1:g.56788_56789del

Transcript Alleles

HGVS Amino-acid Change
ENST00000265362.9:c.113-8163_113-8162del MANE Select ENSP00000265362.3:n.113-8163_113-8162del
ENST00000265362.8:c.113-8163_113-8162del ENSP00000265362.3:n.113-8163_113-8162del
ENST00000420047.1:c.113-8163_113-8162del ENSP00000391900.1:n.113-8163_113-8162del
ENST00000436949.5:c.113-8163_113-8162del ENSP00000415260.1:n.113-8163_113-8162del
NM_006080.2:c.113-8163_113-8162del NP_006071.1:n.113-8163_113-8162del
XM_005250110.2:c.113-8163_113-8162del XP_005250167.1:n.113-8163_113-8162del
XM_005250111.3:c.113-8163_113-8162del XP_005250168.1:n.113-8163_113-8162del
XM_006715839.2:c.113-8163_113-8162del XP_006715902.1:n.113-8163_113-8162del
XM_011515734.1:c.113-8163_113-8162del XP_011514036.1:n.113-8163_113-8162del
XM_011515735.1:c.113-8163_113-8162del XP_011514037.1:n.113-8163_113-8162del
XM_005250110.3:c.113-8163_113-8162del XP_005250167.1:n.113-8163_113-8162del
XM_005250111.4:c.113-8163_113-8162del XP_005250168.1:n.113-8163_113-8162del
XM_006715839.3:c.113-8163_113-8162del XP_006715902.1:n.113-8163_113-8162del
XM_011515734.3:c.113-8163_113-8162del XP_011514036.1:n.113-8163_113-8162del
XM_017011673.1:c.113-8163_113-8162del XP_016867162.1:n.113-8163_113-8162del
XM_024446633.1:c.113-8163_113-8162del XP_024302401.1:n.113-8163_113-8162del
NM_006080.3:c.113-8163_113-8162del MANE Select NP_006071.1:n.113-8163_113-8162del