Canonical Allele Identifier: CA1620016886
Gene: SYNGAP1 HGNC NCBI
SYNGAP1-AS1 HGNC NCBI

Genomic Alleles

HGVS Genome Assembly
NC_000006.12:g.33446635A= , CM000668.2:g.33446635A= GRCh38
NC_000006.11:g.33414412A= , CM000668.1:g.33414412A= GRCh37
NC_000006.10:g.33522390A= NCBI36
NG_016137.1:g.31566A=
NG_016137.2:g.31566A=

Transcript Alleles

HGVS Amino-acid Change
ENST00000682587.1:c.3385A= (SYNGAP1) ENSP00000507403.1:p.Lys1129=
ENST00000418600.7:c.3643A= (SYNGAP1) ENSP00000403636.3:p.Lys1215=
ENST00000449372.7:c.3595A= (SYNGAP1) ENSP00000416519.4:p.Lys1199=
ENST00000629380.3:c.3643A= (SYNGAP1) ENSP00000486463.1:p.Lys1215=
ENST00000644458.1:c.3643A= (SYNGAP1) ENSP00000495541.1:p.Lys1215=
ENST00000645250.1:c.3466A= (SYNGAP1) ENSP00000494861.1:p.Lys1156=
ENST00000646630.1:c.3643A= (SYNGAP1) MANE Select ENSP00000496007.1:p.Lys1215=
ENST00000293748.9:c.3598A= (SYNGAP1) ENSP00000293748.6:p.Lys1200=
ENST00000418600.6:c.3643A= (SYNGAP1) ENSP00000403636.3:p.Lys1215=
ENST00000428982.4:c.3466A= (SYNGAP1) ENSP00000412475.2:p.Lys1156=
ENST00000449372.6:c.3595A= (SYNGAP1) ENSP00000416519.3:p.Lys1199=
ENST00000628646.2:c.3643A= (SYNGAP1) ENSP00000486431.1:p.Lys1215=
ENST00000629380.2:c.3643A= (SYNGAP1) ENSP00000486463.1:p.Lys1215=
NM_006772.2:c.3643A= (SYNGAP1) NP_006763.2:p.Lys1215=
NM_001130066.1:c.3595A= (SYNGAP1) NP_001123538.1:p.Lys1199=
NM_001130066.2:c.3595A= (SYNGAP1) NP_001123538.1:p.Lys1199=
NM_006772.3:c.3643A= (SYNGAP1) MANE Select NP_006763.2:p.Lys1215=
NR_174954.1:n.300T= (SYNGAP1-AS1)