Canonical Allele Identifier: CA1620013490

Gene: SYNGAP1 SYNGAP1-AS1

Genomic Alleles

HGVS	Genome Assembly
NC_000006.12:g.33440737C= , CM000668.2:g.33440737C=	GRCh38
NC_000006.11:g.33408514C= , CM000668.1:g.33408514C=	GRCh37
NC_000006.10:g.33516492C=	NCBI36
NG_016137.1:g.25668C=
NG_016137.2:g.25668C=

Transcript Alleles

HGVS	Amino-acid Change
ENST00000682587.1:c.1427C= (SYNGAP1)	ENSP00000507403.1:p.Pro476=
ENST00000418600.7:c.1685C= (SYNGAP1)	ENSP00000403636.3:p.Pro562=
ENST00000449372.7:c.1685C= (SYNGAP1)	ENSP00000416519.4:p.Pro562=
ENST00000629380.3:c.1685C= (SYNGAP1)	ENSP00000486463.1:p.Pro562=
ENST00000638142.2:c.*82C= (SYNGAP1)	ENSP00000490803.1:n.*82C=
ENST00000644458.1:c.1685C= (SYNGAP1)	ENSP00000495541.1:p.Pro562=
ENST00000645250.1:c.1508C= (SYNGAP1)	ENSP00000494861.1:p.Pro503=
ENST00000646630.1:c.1685C= (SYNGAP1) MANE Select	ENSP00000496007.1:p.Pro562=
ENST00000293748.9:c.1640C= (SYNGAP1)	ENSP00000293748.6:p.Pro547=
ENST00000418600.6:c.1685C= (SYNGAP1)	ENSP00000403636.3:p.Pro562=
ENST00000428982.4:c.1508C= (SYNGAP1)	ENSP00000412475.2:p.Pro503=
ENST00000449372.6:c.1685C= (SYNGAP1)	ENSP00000416519.3:p.Pro562=
ENST00000628646.2:c.1685C= (SYNGAP1)	ENSP00000486431.1:p.Pro562=
ENST00000629380.2:c.1685C= (SYNGAP1)	ENSP00000486463.1:p.Pro562=
NM_006772.2:c.1685C= (SYNGAP1)	NP_006763.2:p.Pro562=
NM_001130066.1:c.1685C= (SYNGAP1)	NP_001123538.1:p.Pro562=
NM_001130066.2:c.1685C= (SYNGAP1)	NP_001123538.1:p.Pro562=
NM_006772.3:c.1685C= (SYNGAP1) MANE Select	NP_006763.2:p.Pro562=
NR_174954.1:n.330-3256G= (SYNGAP1-AS1)