Canonical Allele Identifier: CA16618569
Gene: SEMA3A HGNC NCBI

Linked Data

ClinVar Variation Id: 418484
ClinVar RCV Id: RCV000479871
dbSNP Id: rs1064793265

Genomic Alleles

HGVS Genome Assembly
NC_000007.14:g.83981442G>A , CM000669.2:g.83981442G>A GRCh38
NC_000007.13:g.83610758G>A , CM000669.1:g.83610758G>A GRCh37
NC_000007.12:g.83448694G>A NCBI36
NG_011489.1:g.218460C>T

Transcript Alleles

HGVS Amino-acid change
ENST00000265362.9:c.1531C>T MANE Select ENSP00000265362.3:p.Gln511Ter
ENST00000265362.8:c.1531C>T ENSP00000265362.3:p.Gln511Ter
ENST00000436949.5:c.1531C>T ENSP00000415260.1:p.Gln511Ter
NM_006080.2:c.1531C>T NP_006071.1:p.Gln511Ter
XM_005250110.2:c.1531C>T XP_005250167.1:p.Gln511Ter
XM_005250111.3:c.1531C>T XP_005250168.1:p.Gln511Ter
XM_006715839.2:c.1531C>T XP_006715902.1:p.Gln511Ter
XM_011515734.1:c.1531C>T XP_011514036.1:p.Gln511Ter
XM_011515735.1:c.1531C>T XP_011514037.1:p.Gln511Ter
XM_005250110.3:c.1531C>T XP_005250167.1:p.Gln511Ter
XM_005250111.4:c.1531C>T XP_005250168.1:p.Gln511Ter
XM_006715839.3:c.1531C>T XP_006715902.1:p.Gln511Ter
XM_011515734.3:c.1531C>T XP_011514036.1:p.Gln511Ter
XM_017011673.1:c.1531C>T XP_016867162.1:p.Gln511Ter
XM_024446633.1:c.1531C>T XP_024302401.1:p.Gln511Ter
NM_006080.3:c.1531C>T MANE Select NP_006071.1:p.Gln511Ter