Canonical Allele Identifier: CA363623493

Gene: SYNGAP1 SYNGAP1-AS1

Linked Data

• ClinVar Variation Id: 2585497
• ClinVar RCV Id: RCV003338113
• MyVariant Identifiers: chr6:g.33409428A>G (hg19) ; chr6:g.33441651A>G (hg38)

Genomic Alleles

HGVS	Genome Assembly
NC_000006.12:g.33441651A>G , CM000668.2:g.33441651A>G	GRCh38
NC_000006.11:g.33409428A>G , CM000668.1:g.33409428A>G	GRCh37
NC_000006.10:g.33517406A>G	NCBI36
NG_016137.1:g.26582A>G
NG_016137.2:g.26582A>G

Transcript Alleles

HGVS	Amino-acid Change
ENST00000682587.1:c.1928A>G (SYNGAP1)	ENSP00000507403.1:p.Asn643Ser
ENST00000418600.7:c.2186A>G (SYNGAP1)	ENSP00000403636.3:p.Asn729Ser
ENST00000449372.7:c.2186A>G (SYNGAP1)	ENSP00000416519.4:p.Asn729Ser
ENST00000629380.3:c.2186A>G (SYNGAP1)	ENSP00000486463.1:p.Asn729Ser
ENST00000638142.2:c.*583A>G (SYNGAP1)	ENSP00000490803.1:n.*583A>G
ENST00000644458.1:c.2186A>G (SYNGAP1)	ENSP00000495541.1:p.Asn729Ser
ENST00000645250.1:c.2009A>G (SYNGAP1)	ENSP00000494861.1:p.Asn670Ser
ENST00000646630.1:c.2186A>G (SYNGAP1) MANE Select	ENSP00000496007.1:p.Asn729Ser
ENST00000293748.9:c.2141A>G (SYNGAP1)	ENSP00000293748.6:p.Asn714Ser
ENST00000418600.6:c.2186A>G (SYNGAP1)	ENSP00000403636.3:p.Asn729Ser
ENST00000428982.4:c.2009A>G (SYNGAP1)	ENSP00000412475.2:p.Asn670Ser
ENST00000449372.6:c.2186A>G (SYNGAP1)	ENSP00000416519.3:p.Asn729Ser
ENST00000628646.2:c.2186A>G (SYNGAP1)	ENSP00000486431.1:p.Asn729Ser
ENST00000629380.2:c.2186A>G (SYNGAP1)	ENSP00000486463.1:p.Asn729Ser
NM_006772.2:c.2186A>G (SYNGAP1)	NP_006763.2:p.Asn729Ser
NM_001130066.1:c.2186A>G (SYNGAP1)	NP_001123538.1:p.Asn729Ser
NM_001130066.2:c.2186A>G (SYNGAP1)	NP_001123538.1:p.Asn729Ser
NM_006772.3:c.2186A>G (SYNGAP1) MANE Select	NP_006763.2:p.Asn729Ser
NR_174954.1:n.330-4170T>C (SYNGAP1-AS1)