Canonical Allele Identifier: CA450107290

Gene: SYNGAP1 SYNGAP1-AS1

Linked Data

• dbSNP Id: rs1431486384
• gnomAD v2: 6-33405519-G-T
• gnomAD v4: 6-33437742-G-T
• MyVariant Identifiers: chr6:g.33405519G>T (hg19) ; chr6:g.33437742G>T (hg38)

Genomic Alleles

HGVS	Genome Assembly
NC_000006.12:g.33437742G>T , CM000668.2:g.33437742G>T	GRCh38
NC_000006.11:g.33405519G>T , CM000668.1:g.33405519G>T	GRCh37
NC_000006.10:g.33513497G>T	NCBI36
NG_016137.1:g.22673G>T
NG_016137.2:g.22673G>T

Transcript Alleles

HGVS	Amino-acid Change
ENST00000682587.1:c.579G>T (SYNGAP1)	ENSP00000507403.1:p.Arg193=
ENST00000418600.7:c.837G>T (SYNGAP1)	ENSP00000403636.3:p.Arg279=
ENST00000449372.7:c.837G>T (SYNGAP1)	ENSP00000416519.4:p.Arg279=
ENST00000629380.3:c.837G>T (SYNGAP1)	ENSP00000486463.1:p.Arg279=
ENST00000638142.2:c.837G>T (SYNGAP1)	ENSP00000490803.1:p.Arg279=
ENST00000644458.1:c.837G>T (SYNGAP1)	ENSP00000495541.1:p.Arg279=
ENST00000645250.1:c.660G>T (SYNGAP1)	ENSP00000494861.1:p.Arg220=
ENST00000646630.1:c.837G>T (SYNGAP1) MANE Select	ENSP00000496007.1:p.Arg279=
ENST00000293748.9:c.792G>T (SYNGAP1)	ENSP00000293748.6:p.Arg264=
ENST00000418600.6:c.837G>T (SYNGAP1)	ENSP00000403636.3:p.Arg279=
ENST00000428982.4:c.660G>T (SYNGAP1)	ENSP00000412475.2:p.Arg220=
ENST00000449372.6:c.837G>T (SYNGAP1)	ENSP00000416519.3:p.Arg279=
ENST00000479510.2:n.1032G>T (SYNGAP1)
ENST00000628646.2:c.837G>T (SYNGAP1)	ENSP00000486431.1:p.Arg279=
ENST00000629380.2:c.837G>T (SYNGAP1)	ENSP00000486463.1:p.Arg279=
NM_006772.2:c.837G>T (SYNGAP1)	NP_006763.2:p.Arg279=
NM_001130066.1:c.837G>T (SYNGAP1)	NP_001123538.1:p.Arg279=
NM_001130066.2:c.837G>T (SYNGAP1)	NP_001123538.1:p.Arg279=
NM_006772.3:c.837G>T (SYNGAP1) MANE Select	NP_006763.2:p.Arg279=
NR_174954.1:n.330-261C>A (SYNGAP1-AS1)