Canonical Allele Identifier: CA1103891523

Gene: SEMA3A

Linked Data

• dbSNP Id: rs1789416263
• gnomAD v3: 7-83981492-TTACTGCTGTGACAA-T
• gnomAD v4: 7-83981492-TTACTGCTGTGACAA-T

Genomic Alleles

HGVS	Genome Assembly
NC_000007.14:g.83981493_83981506del , CM000669.2:g.83981493_83981506del	GRCh38
NC_000007.13:g.83610809_83610822del , CM000669.1:g.83610809_83610822del	GRCh37
NC_000007.12:g.83448745_83448758del	NCBI36
NG_011489.1:g.218396_218409del

Transcript Alleles

HGVS	Amino-acid Change
ENST00000265362.9:c.1495-28_1495-15del MANE Select	ENSP00000265362.3:n.1495-28_1495-15del
ENST00000265362.8:c.1495-28_1495-15del	ENSP00000265362.3:n.1495-28_1495-15del
ENST00000436949.5:c.1495-28_1495-15del	ENSP00000415260.1:n.1495-28_1495-15del
NM_006080.2:c.1495-28_1495-15del	NP_006071.1:n.1495-28_1495-15del
XM_005250110.2:c.1495-28_1495-15del	XP_005250167.1:n.1495-28_1495-15del
XM_005250111.3:c.1495-28_1495-15del	XP_005250168.1:n.1495-28_1495-15del
XM_006715839.2:c.1495-28_1495-15del	XP_006715902.1:n.1495-28_1495-15del
XM_011515734.1:c.1495-28_1495-15del	XP_011514036.1:n.1495-28_1495-15del
XM_011515735.1:c.1495-28_1495-15del	XP_011514037.1:n.1495-28_1495-15del
XM_005250110.3:c.1495-28_1495-15del	XP_005250167.1:n.1495-28_1495-15del
XM_005250111.4:c.1495-28_1495-15del	XP_005250168.1:n.1495-28_1495-15del
XM_006715839.3:c.1495-28_1495-15del	XP_006715902.1:n.1495-28_1495-15del
XM_011515734.3:c.1495-28_1495-15del	XP_011514036.1:n.1495-28_1495-15del
XM_017011673.1:c.1495-28_1495-15del	XP_016867162.1:n.1495-28_1495-15del
XM_024446633.1:c.1495-28_1495-15del	XP_024302401.1:n.1495-28_1495-15del
NM_006080.3:c.1495-28_1495-15del MANE Select	NP_006071.1:n.1495-28_1495-15del