Canonical Allele Identifier: CA2678271461
Gene: SYNGAP1 HGNC NCBI

Linked Data

Genomic Alleles

HGVS Genome Assembly
NC_000006.12:g.33432956_33432960del , CM000668.2:g.33432956_33432960del GRCh38
NC_000006.11:g.33400733_33400737del , CM000668.1:g.33400733_33400737del GRCh37
NC_000006.10:g.33508711_33508715del NCBI36
NG_016137.1:g.17887_17891del
NG_016137.2:g.17887_17891del

Transcript Alleles

HGVS Amino-acid Change
ENST00000682587.1:c.251+150_251+154del ENSP00000507403.1:n.251+150_251+154del
ENST00000418600.7:c.509+150_509+154del ENSP00000403636.3:n.509+150_509+154del
ENST00000449372.7:c.509+150_509+154del ENSP00000416519.4:n.509+150_509+154del
ENST00000629380.3:c.509+150_509+154del ENSP00000486463.1:n.509+150_509+154del
ENST00000638142.2:c.509+150_509+154del ENSP00000490803.1:n.509+150_509+154del
ENST00000644458.1:c.509+150_509+154del ENSP00000495541.1:n.509+150_509+154del
ENST00000645250.1:c.332+150_332+154del ENSP00000494861.1:n.332+150_332+154del
ENST00000646630.1:c.509+150_509+154del MANE Select ENSP00000496007.1:n.509+150_509+154del
ENST00000293748.9:c.464+150_464+154del ENSP00000293748.6:n.464+150_464+154del
ENST00000418600.6:c.509+150_509+154del ENSP00000403636.3:n.509+150_509+154del
ENST00000428982.4:c.332+150_332+154del ENSP00000412475.2:n.332+150_332+154del
ENST00000449372.6:c.509+150_509+154del ENSP00000416519.3:n.509+150_509+154del
ENST00000479510.2:n.704+150_704+154del
ENST00000628646.2:c.509+150_509+154del ENSP00000486431.1:n.509+150_509+154del
ENST00000629380.2:c.509+150_509+154del ENSP00000486463.1:n.509+150_509+154del
NM_006772.2:c.509+150_509+154del NP_006763.2:n.509+150_509+154del
NM_001130066.1:c.509+150_509+154del NP_001123538.1:n.509+150_509+154del
NM_001130066.2:c.509+150_509+154del NP_001123538.1:n.509+150_509+154del
NM_006772.3:c.509+150_509+154del MANE Select NP_006763.2:n.509+150_509+154del