Canonical Allele Identifier: CA1620010208

Gene: SYNGAP1

Genomic Alleles

HGVS	Genome Assembly
NC_000006.12:g.33432781C= , CM000668.2:g.33432781C=	GRCh38
NC_000006.11:g.33400558C= , CM000668.1:g.33400558C=	GRCh37
NC_000006.10:g.33508536C=	NCBI36
NG_016137.1:g.17712C=
NG_016137.2:g.17712C=

Transcript Alleles

HGVS	Amino-acid Change
ENST00000682587.1:c.226C=	ENSP00000507403.1:p.Arg76=
ENST00000418600.7:c.484C=	ENSP00000403636.3:p.Arg162=
ENST00000449372.7:c.484C=	ENSP00000416519.4:p.Arg162=
ENST00000629380.3:c.484C=	ENSP00000486463.1:p.Arg162=
ENST00000638142.2:c.484C=	ENSP00000490803.1:p.Arg162=
ENST00000644458.1:c.484C=	ENSP00000495541.1:p.Arg162=
ENST00000645250.1:c.307C=	ENSP00000494861.1:p.Arg103=
ENST00000646630.1:c.484C= MANE Select	ENSP00000496007.1:p.Arg162=
ENST00000293748.9:c.439C=	ENSP00000293748.6:p.Arg147=
ENST00000418600.6:c.484C=	ENSP00000403636.3:p.Arg162=
ENST00000428982.4:c.307C=	ENSP00000412475.2:p.Arg103=
ENST00000449372.6:c.484C=	ENSP00000416519.3:p.Arg162=
ENST00000479510.2:n.679C=
ENST00000628646.2:c.484C=	ENSP00000486431.1:p.Arg162=
ENST00000629380.2:c.484C=	ENSP00000486463.1:p.Arg162=
NM_006772.2:c.484C=	NP_006763.2:p.Arg162=
NM_001130066.1:c.484C=	NP_001123538.1:p.Arg162=
NM_001130066.2:c.484C=	NP_001123538.1:p.Arg162=
NM_006772.3:c.484C= MANE Select	NP_006763.2:p.Arg162=