Canonical Allele Identifier: CA2683561549
Gene: SEMA3A HGNC NCBI

Linked Data

Genomic Alleles

HGVS Genome Assembly
NC_000007.14:g.83981536_83981537insCTG , CM000669.2:g.83981536_83981537insCTG GRCh38
NC_000007.13:g.83610852_83610853insCTG , CM000669.1:g.83610852_83610853insCTG GRCh37
NC_000007.12:g.83448788_83448789insCTG NCBI36
NG_011489.1:g.218365_218366insCAG

Transcript Alleles

HGVS Amino-acid Change
ENST00000265362.9:c.1495-59_1495-58insCAG MANE Select ENSP00000265362.3:n.1495-59_1495-58insCAG
ENST00000265362.8:c.1495-59_1495-58insCAG ENSP00000265362.3:n.1495-59_1495-58insCAG
ENST00000436949.5:c.1495-59_1495-58insCAG ENSP00000415260.1:n.1495-59_1495-58insCAG
NM_006080.2:c.1495-59_1495-58insCAG NP_006071.1:n.1495-59_1495-58insCAG
XM_005250110.2:c.1495-59_1495-58insCAG XP_005250167.1:n.1495-59_1495-58insCAG
XM_005250111.3:c.1495-59_1495-58insCAG XP_005250168.1:n.1495-59_1495-58insCAG
XM_006715839.2:c.1495-59_1495-58insCAG XP_006715902.1:n.1495-59_1495-58insCAG
XM_011515734.1:c.1495-59_1495-58insCAG XP_011514036.1:n.1495-59_1495-58insCAG
XM_011515735.1:c.1495-59_1495-58insCAG XP_011514037.1:n.1495-59_1495-58insCAG
XM_005250110.3:c.1495-59_1495-58insCAG XP_005250167.1:n.1495-59_1495-58insCAG
XM_005250111.4:c.1495-59_1495-58insCAG XP_005250168.1:n.1495-59_1495-58insCAG
XM_006715839.3:c.1495-59_1495-58insCAG XP_006715902.1:n.1495-59_1495-58insCAG
XM_011515734.3:c.1495-59_1495-58insCAG XP_011514036.1:n.1495-59_1495-58insCAG
XM_017011673.1:c.1495-59_1495-58insCAG XP_016867162.1:n.1495-59_1495-58insCAG
XM_024446633.1:c.1495-59_1495-58insCAG XP_024302401.1:n.1495-59_1495-58insCAG
NM_006080.3:c.1495-59_1495-58insCAG MANE Select NP_006071.1:n.1495-59_1495-58insCAG