Canonical Allele Identifier: CA1721974590

Gene: SEMA3A

Genomic Alleles

HGVS	Genome Assembly
NC_000007.14:g.84027474_84027475delinsGT , CM000669.2:g.84027474_84027475delinsGT	GRCh38
NC_000007.13:g.83656790_83656791delinsGT , CM000669.1:g.83656790_83656791delinsGT	GRCh37
NC_000007.12:g.83494726_83494727delinsGT	NCBI36
NG_011489.1:g.172427_172428delinsAC

Transcript Alleles

HGVS	Amino-acid Change
ENST00000265362.9:c.668-13124_668-13123delinsAC MANE Select	ENSP00000265362.3:n.668-13124_668-13123delinsAC
ENST00000265362.8:c.668-13124_668-13123delinsAC	ENSP00000265362.3:n.668-13124_668-13123delinsAC
ENST00000436949.5:c.668-13124_668-13123delinsAC	ENSP00000415260.1:n.668-13124_668-13123delinsAC
NM_006080.2:c.668-13124_668-13123delinsAC	NP_006071.1:n.668-13124_668-13123delinsAC
XM_005250110.2:c.668-13124_668-13123delinsAC	XP_005250167.1:n.668-13124_668-13123delinsAC
XM_005250111.3:c.668-13124_668-13123delinsAC	XP_005250168.1:n.668-13124_668-13123delinsAC
XM_006715839.2:c.668-13124_668-13123delinsAC	XP_006715902.1:n.668-13124_668-13123delinsAC
XM_011515734.1:c.668-13124_668-13123delinsAC	XP_011514036.1:n.668-13124_668-13123delinsAC
XM_011515735.1:c.668-13124_668-13123delinsAC	XP_011514037.1:n.668-13124_668-13123delinsAC
XM_005250110.3:c.668-13124_668-13123delinsAC	XP_005250167.1:n.668-13124_668-13123delinsAC
XM_005250111.4:c.668-13124_668-13123delinsAC	XP_005250168.1:n.668-13124_668-13123delinsAC
XM_006715839.3:c.668-13124_668-13123delinsAC	XP_006715902.1:n.668-13124_668-13123delinsAC
XM_011515734.3:c.668-13124_668-13123delinsAC	XP_011514036.1:n.668-13124_668-13123delinsAC
XM_017011673.1:c.668-13124_668-13123delinsAC	XP_016867162.1:n.668-13124_668-13123delinsAC
XM_024446633.1:c.668-13124_668-13123delinsAC	XP_024302401.1:n.668-13124_668-13123delinsAC
NM_006080.3:c.668-13124_668-13123delinsAC MANE Select	NP_006071.1:n.668-13124_668-13123delinsAC