Canonical Allele Identifier: CA1620016693

Gene: SYNGAP1 SYNGAP1-AS1

Genomic Alleles

HGVS	Genome Assembly
NC_000006.12:g.33446493T= , CM000668.2:g.33446493T=	GRCh38
NC_000006.11:g.33414270T= , CM000668.1:g.33414270T=	GRCh37
NC_000006.10:g.33522248T=	NCBI36
NG_016137.1:g.31424T=
NG_016137.2:g.31424T=

Transcript Alleles

HGVS	Amino-acid Change
ENST00000682587.1:c.3325-82T= (SYNGAP1)	ENSP00000507403.1:n.3325-82T=
ENST00000418600.7:c.3583-82T= (SYNGAP1)	ENSP00000403636.3:n.3583-82T=
ENST00000449372.7:c.3541-88T= (SYNGAP1)	ENSP00000416519.4:n.3541-88T=
ENST00000629380.3:c.3583-82T= (SYNGAP1)	ENSP00000486463.1:n.3583-82T=
ENST00000644458.1:c.3583-82T= (SYNGAP1)	ENSP00000495541.1:n.3583-82T=
ENST00000645250.1:c.3406-82T= (SYNGAP1)	ENSP00000494861.1:n.3406-82T=
ENST00000646630.1:c.3583-82T= (SYNGAP1) MANE Select	ENSP00000496007.1:n.3583-82T=
ENST00000293748.9:c.3538-82T= (SYNGAP1)	ENSP00000293748.6:n.3538-82T=
ENST00000418600.6:c.3583-82T= (SYNGAP1)	ENSP00000403636.3:n.3583-82T=
ENST00000428982.4:c.3406-82T= (SYNGAP1)	ENSP00000412475.2:n.3406-82T=
ENST00000449372.6:c.3541-88T= (SYNGAP1)	ENSP00000416519.3:n.3541-88T=
ENST00000628646.2:c.3583-82T= (SYNGAP1)	ENSP00000486431.1:n.3583-82T=
ENST00000629380.2:c.3583-82T= (SYNGAP1)	ENSP00000486463.1:n.3583-82T=
NM_006772.2:c.3583-82T= (SYNGAP1)	NP_006763.2:n.3583-82T=
NM_001130066.1:c.3541-88T= (SYNGAP1)	NP_001123538.1:n.3541-88T=
NM_001130066.2:c.3541-88T= (SYNGAP1)	NP_001123538.1:n.3541-88T=
NM_006772.3:c.3583-82T= (SYNGAP1) MANE Select	NP_006763.2:n.3583-82T=
NR_174954.1:n.329+113A= (SYNGAP1-AS1)