Canonical Allele Identifier: CA843054592

Gene: SEMA3A

Linked Data

• dbSNP Id: rs1322465522
• MyVariant Identifiers: chr7:g.83610278_83610279insTCTC (hg19) ; chr7:g.83980962_83980963insTCTC (hg38)

Genomic Alleles

HGVS	Genome Assembly
NC_000007.14:g.83980964_83980967dup , CM000669.2:g.83980964_83980967dup	GRCh38
NC_000007.13:g.83610280_83610283dup , CM000669.1:g.83610280_83610283dup	GRCh37
NC_000007.12:g.83448216_83448219dup	NCBI36
NG_011489.1:g.218936_218939dup

Transcript Alleles

HGVS	Amino-acid Change
ENST00000265362.9:c.1652+355_1652+358dup MANE Select	ENSP00000265362.3:n.1652+355_1652+358dup
ENST00000265362.8:c.1652+355_1652+358dup	ENSP00000265362.3:n.1652+355_1652+358dup
ENST00000436949.5:c.1652+355_1652+358dup	ENSP00000415260.1:n.1652+355_1652+358dup
NM_006080.2:c.1652+355_1652+358dup	NP_006071.1:n.1652+355_1652+358dup
XM_005250110.2:c.1652+355_1652+358dup	XP_005250167.1:n.1652+355_1652+358dup
XM_005250111.3:c.1652+355_1652+358dup	XP_005250168.1:n.1652+355_1652+358dup
XM_006715839.2:c.1652+355_1652+358dup	XP_006715902.1:n.1652+355_1652+358dup
XM_011515734.1:c.1652+355_1652+358dup	XP_011514036.1:n.1652+355_1652+358dup
XM_011515735.1:c.1652+355_1652+358dup	XP_011514037.1:n.1652+355_1652+358dup
XM_005250110.3:c.1652+355_1652+358dup	XP_005250167.1:n.1652+355_1652+358dup
XM_005250111.4:c.1652+355_1652+358dup	XP_005250168.1:n.1652+355_1652+358dup
XM_006715839.3:c.1652+355_1652+358dup	XP_006715902.1:n.1652+355_1652+358dup
XM_011515734.3:c.1652+355_1652+358dup	XP_011514036.1:n.1652+355_1652+358dup
XM_017011673.1:c.1652+355_1652+358dup	XP_016867162.1:n.1652+355_1652+358dup
XM_024446633.1:c.1652+355_1652+358dup	XP_024302401.1:n.1652+355_1652+358dup
NM_006080.3:c.1652+355_1652+358dup MANE Select	NP_006071.1:n.1652+355_1652+358dup