Canonical Allele Identifier: CA3758797

Gene: SYNGAP1 SYNGAP1-AS1

Linked Data

• dbSNP Id: rs754730641
• ExAC: 6:33409342 A / G
• gnomAD v2: 6-33409342-A-G
• gnomAD v4: 6-33441565-A-G
• MyVariant Identifiers: chr6:g.33409342A>G (hg19) ; chr6:g.33441565A>G (hg38)

Genomic Alleles

HGVS	Genome Assembly
NC_000006.12:g.33441565A>G , CM000668.2:g.33441565A>G	GRCh38
NC_000006.11:g.33409342A>G , CM000668.1:g.33409342A>G	GRCh37
NC_000006.10:g.33517320A>G	NCBI36
NG_016137.1:g.26496A>G
NG_016137.2:g.26496A>G

Transcript Alleles

HGVS	Amino-acid Change
ENST00000682587.1:c.1858-16A>G (SYNGAP1)	ENSP00000507403.1:n.1858-16A>G
ENST00000418600.7:c.2116-16A>G (SYNGAP1)	ENSP00000403636.3:n.2116-16A>G
ENST00000449372.7:c.2116-16A>G (SYNGAP1)	ENSP00000416519.4:n.2116-16A>G
ENST00000629380.3:c.2116-16A>G (SYNGAP1)	ENSP00000486463.1:n.2116-16A>G
ENST00000638142.2:c.*513-16A>G (SYNGAP1)	ENSP00000490803.1:n.*513-16A>G
ENST00000644458.1:c.2116-16A>G (SYNGAP1)	ENSP00000495541.1:n.2116-16A>G
ENST00000645250.1:c.1939-16A>G (SYNGAP1)	ENSP00000494861.1:n.1939-16A>G
ENST00000646630.1:c.2116-16A>G (SYNGAP1) MANE Select	ENSP00000496007.1:n.2116-16A>G
ENST00000293748.9:c.2071-16A>G (SYNGAP1)	ENSP00000293748.6:n.2071-16A>G
ENST00000418600.6:c.2116-16A>G (SYNGAP1)	ENSP00000403636.3:n.2116-16A>G
ENST00000428982.4:c.1939-16A>G (SYNGAP1)	ENSP00000412475.2:n.1939-16A>G
ENST00000449372.6:c.2116-16A>G (SYNGAP1)	ENSP00000416519.3:n.2116-16A>G
ENST00000628646.2:c.2116-16A>G (SYNGAP1)	ENSP00000486431.1:n.2116-16A>G
ENST00000629380.2:c.2116-16A>G (SYNGAP1)	ENSP00000486463.1:n.2116-16A>G
NM_006772.2:c.2116-16A>G (SYNGAP1)	NP_006763.2:n.2116-16A>G
NM_001130066.1:c.2116-16A>G (SYNGAP1)	NP_001123538.1:n.2116-16A>G
NM_001130066.2:c.2116-16A>G (SYNGAP1)	NP_001123538.1:n.2116-16A>G
NM_006772.3:c.2116-16A>G (SYNGAP1) MANE Select	NP_006763.2:n.2116-16A>G
NR_174954.1:n.330-4084T>C (SYNGAP1-AS1)