Canonical Allele Identifier: CA1620014596

Gene: SYNGAP1 SYNGAP1-AS1

Genomic Alleles

HGVS	Genome Assembly
NC_000006.12:g.33443335A= , CM000668.2:g.33443335A=	GRCh38
NC_000006.11:g.33411112A= , CM000668.1:g.33411112A=	GRCh37
NC_000006.10:g.33519090A=	NCBI36
NG_016137.1:g.28266A=
NG_016137.2:g.28266A=

Transcript Alleles

HGVS	Amino-acid Change
ENST00000682587.1:c.2525A= (SYNGAP1)	ENSP00000507403.1:p.Gln842=
ENST00000418600.7:c.2783A= (SYNGAP1)	ENSP00000403636.3:p.Gln928=
ENST00000449372.7:c.2741A= (SYNGAP1)	ENSP00000416519.4:p.Gln914=
ENST00000629380.3:c.2783A= (SYNGAP1)	ENSP00000486463.1:p.Gln928=
ENST00000644458.1:c.2783A= (SYNGAP1)	ENSP00000495541.1:p.Gln928=
ENST00000645250.1:c.2606A= (SYNGAP1)	ENSP00000494861.1:p.Gln869=
ENST00000646630.1:c.2783A= (SYNGAP1) MANE Select	ENSP00000496007.1:p.Gln928=
ENST00000293748.9:c.2738A= (SYNGAP1)	ENSP00000293748.6:p.Gln913=
ENST00000418600.6:c.2783A= (SYNGAP1)	ENSP00000403636.3:p.Gln928=
ENST00000428982.4:c.2606A= (SYNGAP1)	ENSP00000412475.2:p.Gln869=
ENST00000449372.6:c.2741A= (SYNGAP1)	ENSP00000416519.3:p.Gln914=
ENST00000628646.2:c.2783A= (SYNGAP1)	ENSP00000486431.1:p.Gln928=
ENST00000629380.2:c.2783A= (SYNGAP1)	ENSP00000486463.1:p.Gln928=
NM_006772.2:c.2783A= (SYNGAP1)	NP_006763.2:p.Gln928=
NM_001130066.1:c.2741A= (SYNGAP1)	NP_001123538.1:p.Gln914=
NM_001130066.2:c.2741A= (SYNGAP1)	NP_001123538.1:p.Gln914=
NM_006772.3:c.2783A= (SYNGAP1) MANE Select	NP_006763.2:p.Gln928=
NR_174954.1:n.329+3271T= (SYNGAP1-AS1)