Canonical Allele Identifier: CA1620017142

Gene: SYNGAP1 SYNGAP1-AS1

Genomic Alleles

HGVS	Genome Assembly
NC_000006.12:g.33446826_33446827delinsTG , CM000668.2:g.33446826_33446827delinsTG	GRCh38
NC_000006.11:g.33414603_33414604delinsTG , CM000668.1:g.33414603_33414604delinsTG	GRCh37
NC_000006.10:g.33522581_33522582delinsTG	NCBI36
NG_016137.1:g.31757_31758delinsTG
NG_016137.2:g.31757_31758delinsTG

Transcript Alleles

HGVS	Amino-acid Change
ENST00000682587.1:c.3536+40_3536+41delinsTG (SYNGAP1)	ENSP00000507403.1:n.3536+40_3536+41delinsTG
ENST00000418600.7:c.3794+40_3794+41delinsTG (SYNGAP1)	ENSP00000403636.3:n.3794+40_3794+41delinsTG
ENST00000449372.7:c.3746+40_3746+41delinsTG (SYNGAP1)	ENSP00000416519.4:n.3746+40_3746+41delinsTG
ENST00000629380.3:c.3794+40_3794+41delinsTG (SYNGAP1)	ENSP00000486463.1:n.3794+40_3794+41delinsTG
ENST00000636436.1:n.76+40_76+41delinsTG (SYNGAP1)
ENST00000644458.1:c.3794+40_3794+41delinsTG (SYNGAP1)	ENSP00000495541.1:n.3794+40_3794+41delinsTG
ENST00000645250.1:c.3617+40_3617+41delinsTG (SYNGAP1)	ENSP00000494861.1:n.3617+40_3617+41delinsTG
ENST00000646630.1:c.3794+40_3794+41delinsTG (SYNGAP1) MANE Select	ENSP00000496007.1:n.3794+40_3794+41delinsTG
ENST00000293748.9:c.3749+40_3749+41delinsTG (SYNGAP1)	ENSP00000293748.6:n.3749+40_3749+41delinsTG
ENST00000418600.6:c.3794+40_3794+41delinsTG (SYNGAP1)	ENSP00000403636.3:n.3794+40_3794+41delinsTG
ENST00000428982.4:c.3617+40_3617+41delinsTG (SYNGAP1)	ENSP00000412475.2:n.3617+40_3617+41delinsTG
ENST00000449372.6:c.3746+40_3746+41delinsTG (SYNGAP1)	ENSP00000416519.3:n.3746+40_3746+41delinsTG
ENST00000470232.1:n.76+40_76+41delinsTG (SYNGAP1)
ENST00000628646.2:c.3794+40_3794+41delinsTG (SYNGAP1)	ENSP00000486431.1:n.3794+40_3794+41delinsTG
ENST00000629380.2:c.3794+40_3794+41delinsTG (SYNGAP1)	ENSP00000486463.1:n.3794+40_3794+41delinsTG
NM_006772.2:c.3794+40_3794+41delinsTG (SYNGAP1)	NP_006763.2:n.3794+40_3794+41delinsTG
NM_001130066.1:c.3746+40_3746+41delinsTG (SYNGAP1)	NP_001123538.1:n.3746+40_3746+41delinsTG
NM_001130066.2:c.3746+40_3746+41delinsTG (SYNGAP1)	NP_001123538.1:n.3746+40_3746+41delinsTG
NM_006772.3:c.3794+40_3794+41delinsTG (SYNGAP1) MANE Select	NP_006763.2:n.3794+40_3794+41delinsTG
NR_174954.1:n.137-29_137-28delinsCA (SYNGAP1-AS1)