Canonical Allele Identifier: CA2695202918

Gene: SYNGAP1 SYNGAP1-AS1

Genomic Alleles

HGVS	Genome Assembly
NC_000006.12:g.33443181_33443182del , CM000668.2:g.33443181_33443182del	GRCh38
NC_000006.11:g.33410958_33410959del , CM000668.1:g.33410958_33410959del	GRCh37
NC_000006.10:g.33518936_33518937del	NCBI36
NG_016137.1:g.28112_28113del
NG_016137.2:g.28112_28113del

Transcript Alleles

HGVS	Amino-acid Change
ENST00000682587.1:c.2371_2372del (SYNGAP1)	ENSP00000507403.1:p.Leu791AspfsTer?
ENST00000418600.7:c.2629_2630del (SYNGAP1)	ENSP00000403636.3:p.Leu877AspfsTer?
ENST00000449372.7:c.2587_2588del (SYNGAP1)	ENSP00000416519.4:p.Leu863AspfsTer?
ENST00000629380.3:c.2629_2630del (SYNGAP1)	ENSP00000486463.1:p.Leu877AspfsTer?
ENST00000644458.1:c.2629_2630del (SYNGAP1)	ENSP00000495541.1:p.Leu877AspfsTer?
ENST00000645250.1:c.2452_2453del (SYNGAP1)	ENSP00000494861.1:p.Leu818AspfsTer?
ENST00000646630.1:c.2629_2630del (SYNGAP1) MANE Select	ENSP00000496007.1:p.Leu877AspfsTer?
ENST00000293748.9:c.2584_2585del (SYNGAP1)	ENSP00000293748.6:p.Leu862AspfsTer?
ENST00000418600.6:c.2629_2630del (SYNGAP1)	ENSP00000403636.3:p.Leu877AspfsTer?
ENST00000428982.4:c.2452_2453del (SYNGAP1)	ENSP00000412475.2:p.Leu818AspfsTer?
ENST00000449372.6:c.2587_2588del (SYNGAP1)	ENSP00000416519.3:p.Leu863AspfsTer?
ENST00000628646.2:c.2629_2630del (SYNGAP1)	ENSP00000486431.1:p.Leu877AspfsTer?
ENST00000629380.2:c.2629_2630del (SYNGAP1)	ENSP00000486463.1:p.Leu877AspfsTer?
NM_006772.2:c.2629_2630del (SYNGAP1)	NP_006763.2:p.Leu877AspfsTer?
NM_001130066.1:c.2587_2588del (SYNGAP1)	NP_001123538.1:p.Leu863AspfsTer?
NM_001130066.2:c.2587_2588del (SYNGAP1)	NP_001123538.1:p.Leu863AspfsTer?
NM_006772.3:c.2629_2630del (SYNGAP1) MANE Select	NP_006763.2:p.Leu877AspfsTer?
NR_174954.1:n.329+3424_329+3425del (SYNGAP1-AS1)