Canonical Allele Identifier: CA1103891358
Gene: SEMA3A HGNC NCBI

Linked Data

dbSNP Id: rs1318795572

Genomic Alleles

HGVS Genome Assembly
NC_000007.14:g.83981025_83981028dup , CM000669.2:g.83981025_83981028dup GRCh38
NC_000007.13:g.83610341_83610344dup , CM000669.1:g.83610341_83610344dup GRCh37
NC_000007.12:g.83448277_83448280dup NCBI36
NG_011489.1:g.218877_218880dup

Transcript Alleles

HGVS Amino-acid Change
ENST00000265362.9:c.1652+296_1652+299dup MANE Select ENSP00000265362.3:n.1652+296_1652+299dup
ENST00000265362.8:c.1652+296_1652+299dup ENSP00000265362.3:n.1652+296_1652+299dup
ENST00000436949.5:c.1652+296_1652+299dup ENSP00000415260.1:n.1652+296_1652+299dup
NM_006080.2:c.1652+296_1652+299dup NP_006071.1:n.1652+296_1652+299dup
XM_005250110.2:c.1652+296_1652+299dup XP_005250167.1:n.1652+296_1652+299dup
XM_005250111.3:c.1652+296_1652+299dup XP_005250168.1:n.1652+296_1652+299dup
XM_006715839.2:c.1652+296_1652+299dup XP_006715902.1:n.1652+296_1652+299dup
XM_011515734.1:c.1652+296_1652+299dup XP_011514036.1:n.1652+296_1652+299dup
XM_011515735.1:c.1652+296_1652+299dup XP_011514037.1:n.1652+296_1652+299dup
XM_005250110.3:c.1652+296_1652+299dup XP_005250167.1:n.1652+296_1652+299dup
XM_005250111.4:c.1652+296_1652+299dup XP_005250168.1:n.1652+296_1652+299dup
XM_006715839.3:c.1652+296_1652+299dup XP_006715902.1:n.1652+296_1652+299dup
XM_011515734.3:c.1652+296_1652+299dup XP_011514036.1:n.1652+296_1652+299dup
XM_017011673.1:c.1652+296_1652+299dup XP_016867162.1:n.1652+296_1652+299dup
XM_024446633.1:c.1652+296_1652+299dup XP_024302401.1:n.1652+296_1652+299dup
NM_006080.3:c.1652+296_1652+299dup MANE Select NP_006071.1:n.1652+296_1652+299dup