Canonical Allele Identifier: CA843055100

Gene: SEMA3A

Linked Data

• dbSNP Id: rs1302564453
• gnomAD v4: 7-83981575-ATAAAT-A
• MyVariant Identifiers: chr7:g.83610892_83610896del (hg19) ; chr7:g.83981576_83981580del (hg38)

Genomic Alleles

HGVS	Genome Assembly
NC_000007.14:g.83981579_83981583del , CM000669.2:g.83981579_83981583del	GRCh38
NC_000007.13:g.83610895_83610899del , CM000669.1:g.83610895_83610899del	GRCh37
NC_000007.12:g.83448831_83448835del	NCBI36
NG_011489.1:g.218322_218326del

Transcript Alleles

HGVS	Amino-acid Change
ENST00000265362.9:c.1495-102_1495-98del MANE Select	ENSP00000265362.3:n.1495-102_1495-98del
ENST00000265362.8:c.1495-102_1495-98del	ENSP00000265362.3:n.1495-102_1495-98del
ENST00000436949.5:c.1495-102_1495-98del	ENSP00000415260.1:n.1495-102_1495-98del
NM_006080.2:c.1495-102_1495-98del	NP_006071.1:n.1495-102_1495-98del
XM_005250110.2:c.1495-102_1495-98del	XP_005250167.1:n.1495-102_1495-98del
XM_005250111.3:c.1495-102_1495-98del	XP_005250168.1:n.1495-102_1495-98del
XM_006715839.2:c.1495-102_1495-98del	XP_006715902.1:n.1495-102_1495-98del
XM_011515734.1:c.1495-102_1495-98del	XP_011514036.1:n.1495-102_1495-98del
XM_011515735.1:c.1495-102_1495-98del	XP_011514037.1:n.1495-102_1495-98del
XM_005250110.3:c.1495-102_1495-98del	XP_005250167.1:n.1495-102_1495-98del
XM_005250111.4:c.1495-102_1495-98del	XP_005250168.1:n.1495-102_1495-98del
XM_006715839.3:c.1495-102_1495-98del	XP_006715902.1:n.1495-102_1495-98del
XM_011515734.3:c.1495-102_1495-98del	XP_011514036.1:n.1495-102_1495-98del
XM_017011673.1:c.1495-102_1495-98del	XP_016867162.1:n.1495-102_1495-98del
XM_024446633.1:c.1495-102_1495-98del	XP_024302401.1:n.1495-102_1495-98del
NM_006080.3:c.1495-102_1495-98del MANE Select	NP_006071.1:n.1495-102_1495-98del