Canonical Allele Identifier: CA363681960

Gene: SYNGAP1

Linked Data

• ClinVar Variation Id: 39664
• ClinVar RCV Id: RCV000032868
• dbSNP Id: rs2151161019
• MyVariant Identifiers: chr6:g.33402928G>A (hg19) ; chr6:g.33435151G>A (hg38)
• PubMed: PMID:23033978

Genomic Alleles

HGVS	Genome Assembly
NC_000006.12:g.33435151G>A , CM000668.2:g.33435151G>A	GRCh38
NC_000006.11:g.33402928G>A , CM000668.1:g.33402928G>A	GRCh37
NC_000006.10:g.33510906G>A	NCBI36
NG_016137.1:g.20082G>A
NG_016137.2:g.20082G>A

Transcript Alleles

HGVS	Amino-acid change
ENST00000682587.1:c.252-1G>A	ENSP00000507403.1:n.252-1G>A
ENST00000418600.7:c.510-1G>A	ENSP00000403636.3:n.510-1G>A
ENST00000449372.7:c.510-1G>A	ENSP00000416519.4:n.510-1G>A
ENST00000629380.3:c.510-1G>A	ENSP00000486463.1:n.510-1G>A
ENST00000638142.2:c.510-1G>A	ENSP00000490803.1:n.510-1G>A
ENST00000644458.1:c.510-1G>A	ENSP00000495541.1:n.510-1G>A
ENST00000645250.1:c.333-1G>A	ENSP00000494861.1:n.333-1G>A
ENST00000646630.1:c.510-1G>A MANE Select	ENSP00000496007.1:n.510-1G>A
ENST00000293748.9:c.465-1G>A	ENSP00000293748.6:n.465-1G>A
ENST00000418600.6:c.510-1G>A	ENSP00000403636.3:n.510-1G>A
ENST00000428982.4:c.333-1G>A	ENSP00000412475.2:n.333-1G>A
ENST00000449372.6:c.510-1G>A	ENSP00000416519.3:n.510-1G>A
ENST00000479510.2:n.705-1G>A
ENST00000628646.2:c.510-1G>A	ENSP00000486431.1:n.510-1G>A
ENST00000629380.2:c.510-1G>A	ENSP00000486463.1:n.510-1G>A
NM_006772.2:c.510-1G>A	NP_006763.2:n.510-1G>A
NM_001130066.1:c.510-1G>A	NP_001123538.1:n.510-1G>A
NM_001130066.2:c.510-1G>A	NP_001123538.1:n.510-1G>A
NM_006772.3:c.510-1G>A MANE Select	NP_006763.2:n.510-1G>A