Canonical Allele Identifier: CA449860356

Gene: SYNGAP1

Linked Data

• MyVariant Identifiers: chr6:g.33400518C>G (hg19)

Genomic Alleles

HGVS	Genome Assembly
NC_000006.12:g.33432741C>G , CM000668.2:g.33432741C>G	GRCh38
NC_000006.11:g.33400518C>G , CM000668.1:g.33400518C>G	GRCh37
NC_000006.10:g.33508496C>G	NCBI36
NG_016137.1:g.17672C>G
NG_016137.2:g.17672C>G

Transcript Alleles

HGVS	Amino-acid Change
ENST00000682587.1:c.186C>G	ENSP00000507403.1:p.Pro62=
ENST00000418600.7:c.444C>G	ENSP00000403636.3:p.Pro148=
ENST00000449372.7:c.444C>G	ENSP00000416519.4:p.Pro148=
ENST00000629380.3:c.444C>G	ENSP00000486463.1:p.Pro148=
ENST00000638142.2:c.444C>G	ENSP00000490803.1:p.Pro148=
ENST00000644458.1:c.444C>G	ENSP00000495541.1:p.Pro148=
ENST00000645250.1:c.267C>G	ENSP00000494861.1:p.Pro89=
ENST00000646630.1:c.444C>G MANE Select	ENSP00000496007.1:p.Pro148=
ENST00000293748.9:c.399C>G	ENSP00000293748.6:p.Pro133=
ENST00000418600.6:c.444C>G	ENSP00000403636.3:p.Pro148=
ENST00000428982.4:c.267C>G	ENSP00000412475.2:p.Pro89=
ENST00000449372.6:c.444C>G	ENSP00000416519.3:p.Pro148=
ENST00000479510.2:n.639C>G
ENST00000628646.2:c.444C>G	ENSP00000486431.1:p.Pro148=
ENST00000629380.2:c.444C>G	ENSP00000486463.1:p.Pro148=
NM_006772.2:c.444C>G	NP_006763.2:p.Pro148=
NM_001130066.1:c.444C>G	NP_001123538.1:p.Pro148=
NM_001130066.2:c.444C>G	NP_001123538.1:p.Pro148=
NM_006772.3:c.444C>G MANE Select	NP_006763.2:p.Pro148=