Canonical Allele Identifier: CA1620010071

Gene: SYNGAP1

Linked Data

• dbSNP Id: rs1777186428

Genomic Alleles

HGVS	Genome Assembly
NC_000006.12:g.33432538_33432541del , CM000668.2:g.33432538_33432541del	GRCh38
NC_000006.11:g.33400315_33400318del , CM000668.1:g.33400315_33400318del	GRCh37
NC_000006.10:g.33508293_33508296del	NCBI36
NG_016137.1:g.17469_17472del
NG_016137.2:g.17469_17472del

Transcript Alleles

HGVS	Amino-acid Change
ENST00000682587.1:c.130-147_130-144del	ENSP00000507403.1:n.130-147_130-144del
ENST00000418600.7:c.388-147_388-144del	ENSP00000403636.3:n.388-147_388-144del
ENST00000449372.7:c.388-147_388-144del	ENSP00000416519.4:n.388-147_388-144del
ENST00000629380.3:c.388-147_388-144del	ENSP00000486463.1:n.388-147_388-144del
ENST00000638142.2:c.388-147_388-144del	ENSP00000490803.1:n.388-147_388-144del
ENST00000644458.1:c.388-147_388-144del	ENSP00000495541.1:n.388-147_388-144del
ENST00000645250.1:c.211-147_211-144del	ENSP00000494861.1:n.211-147_211-144del
ENST00000646630.1:c.388-147_388-144del MANE Select	ENSP00000496007.1:n.388-147_388-144del
ENST00000293748.9:c.343-147_343-144del	ENSP00000293748.6:n.343-147_343-144del
ENST00000418600.6:c.388-147_388-144del	ENSP00000403636.3:n.388-147_388-144del
ENST00000428982.4:c.211-147_211-144del	ENSP00000412475.2:n.211-147_211-144del
ENST00000449372.6:c.388-147_388-144del	ENSP00000416519.3:n.388-147_388-144del
ENST00000479510.2:n.583-147_583-144del
ENST00000628646.2:c.388-147_388-144del	ENSP00000486431.1:n.388-147_388-144del
ENST00000629380.2:c.388-147_388-144del	ENSP00000486463.1:n.388-147_388-144del
NM_006772.2:c.388-147_388-144del	NP_006763.2:n.388-147_388-144del
NM_001130066.1:c.388-147_388-144del	NP_001123538.1:n.388-147_388-144del
NM_001130066.2:c.388-147_388-144del	NP_001123538.1:n.388-147_388-144del
NM_006772.3:c.388-147_388-144del MANE Select	NP_006763.2:n.388-147_388-144del