Canonical Allele Identifier: CA891842747

Gene: SYNGAP1 SYNGAP1-AS1

Linked Data

• ClinVar Variation Id: 582839
• ClinVar RCV Id: RCV000707018
• dbSNP Id: rs1561784560
• MyVariant Identifiers: chr6:g.33405560del (hg19) ; chr6:g.33437783del (hg38)

Genomic Alleles

HGVS	Genome Assembly
NC_000006.12:g.33437783del , CM000668.2:g.33437783del	GRCh38
NC_000006.11:g.33405560del , CM000668.1:g.33405560del	GRCh37
NC_000006.10:g.33513538del	NCBI36
NG_016137.1:g.22714del
NG_016137.2:g.22714del

Transcript Alleles

HGVS	Amino-acid Change
ENST00000682587.1:c.620del (SYNGAP1)	ENSP00000507403.1:p.Arg207ProfsTer?
ENST00000418600.7:c.878del (SYNGAP1)	ENSP00000403636.3:p.Arg293ProfsTer?
ENST00000449372.7:c.878del (SYNGAP1)	ENSP00000416519.4:p.Arg293ProfsTer?
ENST00000629380.3:c.878del (SYNGAP1)	ENSP00000486463.1:p.Arg293ProfsTer?
ENST00000638142.2:c.878del (SYNGAP1)	ENSP00000490803.1:p.Arg293ProfsTer?
ENST00000644458.1:c.878del (SYNGAP1)	ENSP00000495541.1:p.Arg293ProfsTer?
ENST00000645250.1:c.701del (SYNGAP1)	ENSP00000494861.1:p.Arg234ProfsTer?
ENST00000646630.1:c.878del (SYNGAP1) MANE Select	ENSP00000496007.1:p.Arg293ProfsTer?
ENST00000293748.9:c.833del (SYNGAP1)	ENSP00000293748.6:p.Arg278ProfsTer?
ENST00000418600.6:c.878del (SYNGAP1)	ENSP00000403636.3:p.Arg293ProfsTer?
ENST00000428982.4:c.701del (SYNGAP1)	ENSP00000412475.2:p.Arg234ProfsTer?
ENST00000449372.6:c.878del (SYNGAP1)	ENSP00000416519.3:p.Arg293ProfsTer?
ENST00000479510.2:n.1073del (SYNGAP1)
ENST00000628646.2:c.878del (SYNGAP1)	ENSP00000486431.1:p.Arg293ProfsTer?
ENST00000629380.2:c.878del (SYNGAP1)	ENSP00000486463.1:p.Arg293ProfsTer?
NM_006772.2:c.878del (SYNGAP1)	NP_006763.2:p.Arg293ProfsTer?
NM_001130066.1:c.878del (SYNGAP1)	NP_001123538.1:p.Arg293ProfsTer?
NM_001130066.2:c.878del (SYNGAP1)	NP_001123538.1:p.Arg293ProfsTer?
NM_006772.3:c.878del (SYNGAP1) MANE Select	NP_006763.2:p.Arg293ProfsTer?
NR_174954.1:n.330-302del (SYNGAP1-AS1)