Canonical Allele Identifier: CA363693594

Gene: SYNGAP1 SYNGAP1-AS1

Linked Data

• ClinVar Variation Id: 985418
• ClinVar RCV Id: RCV001266312
• dbSNP Id: rs1761018819
• MyVariant Identifiers: chr6:g.33408643C>G (hg19) ; chr6:g.33440866C>G (hg38)

Genomic Alleles

HGVS	Genome Assembly
NC_000006.12:g.33440866C>G , CM000668.2:g.33440866C>G	GRCh38
NC_000006.11:g.33408643C>G , CM000668.1:g.33408643C>G	GRCh37
NC_000006.10:g.33516621C>G	NCBI36
NG_016137.1:g.25797C>G
NG_016137.2:g.25797C>G

Transcript Alleles

HGVS	Amino-acid change
ENST00000682587.1:c.1556C>G (SYNGAP1)	ENSP00000507403.1:p.Pro519Arg
ENST00000418600.7:c.1814C>G (SYNGAP1)	ENSP00000403636.3:p.Pro605Arg
ENST00000449372.7:c.1814C>G (SYNGAP1)	ENSP00000416519.4:p.Pro605Arg
ENST00000629380.3:c.1814C>G (SYNGAP1)	ENSP00000486463.1:p.Pro605Arg
ENST00000638142.2:c.*211C>G (SYNGAP1)	ENSP00000490803.1:n.*211C>G
ENST00000644458.1:c.1814C>G (SYNGAP1)	ENSP00000495541.1:p.Pro605Arg
ENST00000645250.1:c.1637C>G (SYNGAP1)	ENSP00000494861.1:p.Pro546Arg
ENST00000646630.1:c.1814C>G (SYNGAP1) MANE Select	ENSP00000496007.1:p.Pro605Arg
ENST00000293748.9:c.1769C>G (SYNGAP1)	ENSP00000293748.6:p.Pro590Arg
ENST00000418600.6:c.1814C>G (SYNGAP1)	ENSP00000403636.3:p.Pro605Arg
ENST00000428982.4:c.1637C>G (SYNGAP1)	ENSP00000412475.2:p.Pro546Arg
ENST00000449372.6:c.1814C>G (SYNGAP1)	ENSP00000416519.3:p.Pro605Arg
ENST00000628646.2:c.1814C>G (SYNGAP1)	ENSP00000486431.1:p.Pro605Arg
ENST00000629380.2:c.1814C>G (SYNGAP1)	ENSP00000486463.1:p.Pro605Arg
NM_006772.2:c.1814C>G (SYNGAP1)	NP_006763.2:p.Pro605Arg
NM_001130066.1:c.1814C>G (SYNGAP1)	NP_001123538.1:p.Pro605Arg
NM_001130066.2:c.1814C>G (SYNGAP1)	NP_001123538.1:p.Pro605Arg
NM_006772.3:c.1814C>G (SYNGAP1) MANE Select	NP_006763.2:p.Pro605Arg
NR_174954.1:n.330-3385G>C (SYNGAP1-AS1)