Canonical Allele Identifier: CA1620011288

Gene: SYNGAP1

Genomic Alleles

HGVS	Genome Assembly
NC_000006.12:g.33435113_33435114delinsGC , CM000668.2:g.33435113_33435114delinsGC	GRCh38
NC_000006.11:g.33402890_33402891delinsGC , CM000668.1:g.33402890_33402891delinsGC	GRCh37
NC_000006.10:g.33510868_33510869delinsGC	NCBI36
NG_016137.1:g.20044_20045delinsGC
NG_016137.2:g.20044_20045delinsGC

Transcript Alleles

HGVS	Amino-acid Change
ENST00000682587.1:c.252-39_252-38delinsGC	ENSP00000507403.1:n.252-39_252-38delinsGC
ENST00000418600.7:c.510-39_510-38delinsGC	ENSP00000403636.3:n.510-39_510-38delinsGC
ENST00000449372.7:c.510-39_510-38delinsGC	ENSP00000416519.4:n.510-39_510-38delinsGC
ENST00000629380.3:c.510-39_510-38delinsGC	ENSP00000486463.1:n.510-39_510-38delinsGC
ENST00000638142.2:c.510-39_510-38delinsGC	ENSP00000490803.1:n.510-39_510-38delinsGC
ENST00000644458.1:c.510-39_510-38delinsGC	ENSP00000495541.1:n.510-39_510-38delinsGC
ENST00000645250.1:c.333-39_333-38delinsGC	ENSP00000494861.1:n.333-39_333-38delinsGC
ENST00000646630.1:c.510-39_510-38delinsGC MANE Select	ENSP00000496007.1:n.510-39_510-38delinsGC
ENST00000293748.9:c.465-39_465-38delinsGC	ENSP00000293748.6:n.465-39_465-38delinsGC
ENST00000418600.6:c.510-39_510-38delinsGC	ENSP00000403636.3:n.510-39_510-38delinsGC
ENST00000428982.4:c.333-39_333-38delinsGC	ENSP00000412475.2:n.333-39_333-38delinsGC
ENST00000449372.6:c.510-39_510-38delinsGC	ENSP00000416519.3:n.510-39_510-38delinsGC
ENST00000479510.2:n.705-39_705-38delinsGC
ENST00000628646.2:c.510-39_510-38delinsGC	ENSP00000486431.1:n.510-39_510-38delinsGC
ENST00000629380.2:c.510-39_510-38delinsGC	ENSP00000486463.1:n.510-39_510-38delinsGC
NM_006772.2:c.510-39_510-38delinsGC	NP_006763.2:n.510-39_510-38delinsGC
NM_001130066.1:c.510-39_510-38delinsGC	NP_001123538.1:n.510-39_510-38delinsGC
NM_001130066.2:c.510-39_510-38delinsGC	NP_001123538.1:n.510-39_510-38delinsGC
NM_006772.3:c.510-39_510-38delinsGC MANE Select	NP_006763.2:n.510-39_510-38delinsGC