Canonical Allele Identifier: CA363682192
Gene: SYNGAP1 HGNC NCBI

Linked Data

Genomic Alleles

HGVS Genome Assembly
NC_000006.12:g.33435251T>A , CM000668.2:g.33435251T>A GRCh38
NC_000006.11:g.33403028T>A , CM000668.1:g.33403028T>A GRCh37
NC_000006.10:g.33511006T>A NCBI36
NG_016137.1:g.20182T>A
NG_016137.2:g.20182T>A

Transcript Alleles

HGVS Amino-acid Change
ENST00000682587.1:c.351T>A ENSP00000507403.1:p.Asp117Glu
ENST00000418600.7:c.609T>A ENSP00000403636.3:p.Asp203Glu
ENST00000449372.7:c.609T>A ENSP00000416519.4:p.Asp203Glu
ENST00000629380.3:c.609T>A ENSP00000486463.1:p.Asp203Glu
ENST00000638142.2:c.609T>A ENSP00000490803.1:p.Asp203Glu
ENST00000644458.1:c.609T>A ENSP00000495541.1:p.Asp203Glu
ENST00000645250.1:c.432T>A ENSP00000494861.1:p.Asp144Glu
ENST00000646630.1:c.609T>A MANE Select ENSP00000496007.1:p.Asp203Glu
ENST00000293748.9:c.564T>A ENSP00000293748.6:p.Asp188Glu
ENST00000418600.6:c.609T>A ENSP00000403636.3:p.Asp203Glu
ENST00000428982.4:c.432T>A ENSP00000412475.2:p.Asp144Glu
ENST00000449372.6:c.609T>A ENSP00000416519.3:p.Asp203Glu
ENST00000479510.2:n.804T>A
ENST00000628646.2:c.609T>A ENSP00000486431.1:p.Asp203Glu
ENST00000629380.2:c.609T>A ENSP00000486463.1:p.Asp203Glu
NM_006772.2:c.609T>A NP_006763.2:p.Asp203Glu
NM_001130066.1:c.609T>A NP_001123538.1:p.Asp203Glu
NM_001130066.2:c.609T>A NP_001123538.1:p.Asp203Glu
NM_006772.3:c.609T>A MANE Select NP_006763.2:p.Asp203Glu