Canonical Allele Identifier: CA1620011300
Gene: SYNGAP1 HGNC NCBI

Genomic Alleles

HGVS Genome Assembly
NC_000006.12:g.33435153G= , CM000668.2:g.33435153G= GRCh38
NC_000006.11:g.33402930G= , CM000668.1:g.33402930G= GRCh37
NC_000006.10:g.33510908G= NCBI36
NG_016137.1:g.20084G=
NG_016137.2:g.20084G=

Transcript Alleles

HGVS Amino-acid change
ENST00000682587.1:c.253G= ENSP00000507403.1:p.Ala85=
ENST00000418600.7:c.511G= ENSP00000403636.3:p.Ala171=
ENST00000449372.7:c.511G= ENSP00000416519.4:p.Ala171=
ENST00000629380.3:c.511G= ENSP00000486463.1:p.Ala171=
ENST00000638142.2:c.511G= ENSP00000490803.1:p.Ala171=
ENST00000644458.1:c.511G= ENSP00000495541.1:p.Ala171=
ENST00000645250.1:c.334G= ENSP00000494861.1:p.Ala112=
ENST00000646630.1:c.511G= MANE Select ENSP00000496007.1:p.Ala171=
ENST00000293748.9:c.466G= ENSP00000293748.6:p.Ala156=
ENST00000418600.6:c.511G= ENSP00000403636.3:p.Ala171=
ENST00000428982.4:c.334G= ENSP00000412475.2:p.Ala112=
ENST00000449372.6:c.511G= ENSP00000416519.3:p.Ala171=
ENST00000479510.2:n.706G=
ENST00000628646.2:c.511G= ENSP00000486431.1:p.Ala171=
ENST00000629380.2:c.511G= ENSP00000486463.1:p.Ala171=
NM_006772.2:c.511G= NP_006763.2:p.Ala171=
NM_001130066.1:c.511G= NP_001123538.1:p.Ala171=
NM_001130066.2:c.511G= NP_001123538.1:p.Ala171=
NM_006772.3:c.511G= MANE Select NP_006763.2:p.Ala171=