Canonical Allele Identifier: CA1620011302
Gene: SYNGAP1 HGNC NCBI

Genomic Alleles

HGVS Genome Assembly
NC_000006.12:g.33435156C= , CM000668.2:g.33435156C= GRCh38
NC_000006.11:g.33402933C= , CM000668.1:g.33402933C= GRCh37
NC_000006.10:g.33510911C= NCBI36
NG_016137.1:g.20087C=
NG_016137.2:g.20087C=

Transcript Alleles

HGVS Amino-acid change
ENST00000682587.1:c.256C= ENSP00000507403.1:p.Arg86=
ENST00000418600.7:c.514C= ENSP00000403636.3:p.Arg172=
ENST00000449372.7:c.514C= ENSP00000416519.4:p.Arg172=
ENST00000629380.3:c.514C= ENSP00000486463.1:p.Arg172=
ENST00000638142.2:c.514C= ENSP00000490803.1:p.Arg172=
ENST00000644458.1:c.514C= ENSP00000495541.1:p.Arg172=
ENST00000645250.1:c.337C= ENSP00000494861.1:p.Arg113=
ENST00000646630.1:c.514C= MANE Select ENSP00000496007.1:p.Arg172=
ENST00000293748.9:c.469C= ENSP00000293748.6:p.Arg157=
ENST00000418600.6:c.514C= ENSP00000403636.3:p.Arg172=
ENST00000428982.4:c.337C= ENSP00000412475.2:p.Arg113=
ENST00000449372.6:c.514C= ENSP00000416519.3:p.Arg172=
ENST00000479510.2:n.709C=
ENST00000628646.2:c.514C= ENSP00000486431.1:p.Arg172=
ENST00000629380.2:c.514C= ENSP00000486463.1:p.Arg172=
NM_006772.2:c.514C= NP_006763.2:p.Arg172=
NM_001130066.1:c.514C= NP_001123538.1:p.Arg172=
NM_001130066.2:c.514C= NP_001123538.1:p.Arg172=
NM_006772.3:c.514C= MANE Select NP_006763.2:p.Arg172=