Canonical Allele Identifier: CA575828878

Gene: SEMA3A

Linked Data

• dbSNP Id: rs1277449582
• gnomAD v2: 7-83610587-C-CAGAT
• gnomAD v3: 7-83981271-C-CAGAT
• gnomAD v4: 7-83981271-C-CAGAT
• MyVariant Identifiers: chr7:g.83610587_83610588insAGAT (hg19) ; chr7:g.83981271_83981272insAGAT (hg38)

Genomic Alleles

HGVS	Genome Assembly
NC_000007.14:g.83981274_83981277dup , CM000669.2:g.83981274_83981277dup	GRCh38
NC_000007.13:g.83610590_83610593dup , CM000669.1:g.83610590_83610593dup	GRCh37
NC_000007.12:g.83448526_83448529dup	NCBI36
NG_011489.1:g.218627_218630dup

Transcript Alleles

HGVS	Amino-acid Change
ENST00000265362.9:c.1652+46_1652+49dup MANE Select	ENSP00000265362.3:n.1652+46_1652+49dup
ENST00000265362.8:c.1652+46_1652+49dup	ENSP00000265362.3:n.1652+46_1652+49dup
ENST00000436949.5:c.1652+46_1652+49dup	ENSP00000415260.1:n.1652+46_1652+49dup
NM_006080.2:c.1652+46_1652+49dup	NP_006071.1:n.1652+46_1652+49dup
XM_005250110.2:c.1652+46_1652+49dup	XP_005250167.1:n.1652+46_1652+49dup
XM_005250111.3:c.1652+46_1652+49dup	XP_005250168.1:n.1652+46_1652+49dup
XM_006715839.2:c.1652+46_1652+49dup	XP_006715902.1:n.1652+46_1652+49dup
XM_011515734.1:c.1652+46_1652+49dup	XP_011514036.1:n.1652+46_1652+49dup
XM_011515735.1:c.1652+46_1652+49dup	XP_011514037.1:n.1652+46_1652+49dup
XM_005250110.3:c.1652+46_1652+49dup	XP_005250167.1:n.1652+46_1652+49dup
XM_005250111.4:c.1652+46_1652+49dup	XP_005250168.1:n.1652+46_1652+49dup
XM_006715839.3:c.1652+46_1652+49dup	XP_006715902.1:n.1652+46_1652+49dup
XM_011515734.3:c.1652+46_1652+49dup	XP_011514036.1:n.1652+46_1652+49dup
XM_017011673.1:c.1652+46_1652+49dup	XP_016867162.1:n.1652+46_1652+49dup
XM_024446633.1:c.1652+46_1652+49dup	XP_024302401.1:n.1652+46_1652+49dup
NM_006080.3:c.1652+46_1652+49dup MANE Select	NP_006071.1:n.1652+46_1652+49dup