Canonical Allele Identifier: CA363631283

Gene: SYNGAP1 SYNGAP1-AS1

Linked Data

• MyVariant Identifiers: chr6:g.33411442C>T (hg19) ; chr6:g.33443665C>T (hg38)

Genomic Alleles

HGVS	Genome Assembly
NC_000006.12:g.33443665C>T , CM000668.2:g.33443665C>T	GRCh38
NC_000006.11:g.33411442C>T , CM000668.1:g.33411442C>T	GRCh37
NC_000006.10:g.33519420C>T	NCBI36
NG_016137.1:g.28596C>T
NG_016137.2:g.28596C>T

Transcript Alleles

HGVS	Amino-acid change
ENST00000682587.1:c.2855C>T (SYNGAP1)	ENSP00000507403.1:p.Thr952Ile
ENST00000418600.7:c.3113C>T (SYNGAP1)	ENSP00000403636.3:p.Thr1038Ile
ENST00000449372.7:c.3071C>T (SYNGAP1)	ENSP00000416519.4:p.Thr1024Ile
ENST00000629380.3:c.3113C>T (SYNGAP1)	ENSP00000486463.1:p.Thr1038Ile
ENST00000644458.1:c.3113C>T (SYNGAP1)	ENSP00000495541.1:p.Thr1038Ile
ENST00000645250.1:c.2936C>T (SYNGAP1)	ENSP00000494861.1:p.Thr979Ile
ENST00000646630.1:c.3113C>T (SYNGAP1) MANE Select	ENSP00000496007.1:p.Thr1038Ile
ENST00000293748.9:c.3068C>T (SYNGAP1)	ENSP00000293748.6:p.Thr1023Ile
ENST00000418600.6:c.3113C>T (SYNGAP1)	ENSP00000403636.3:p.Thr1038Ile
ENST00000428982.4:c.2936C>T (SYNGAP1)	ENSP00000412475.2:p.Thr979Ile
ENST00000449372.6:c.3071C>T (SYNGAP1)	ENSP00000416519.3:p.Thr1024Ile
ENST00000628646.2:c.3113C>T (SYNGAP1)	ENSP00000486431.1:p.Thr1038Ile
ENST00000629380.2:c.3113C>T (SYNGAP1)	ENSP00000486463.1:p.Thr1038Ile
NM_006772.2:c.3113C>T (SYNGAP1)	NP_006763.2:p.Thr1038Ile
NM_001130066.1:c.3071C>T (SYNGAP1)	NP_001123538.1:p.Thr1024Ile
NM_001130066.2:c.3071C>T (SYNGAP1)	NP_001123538.1:p.Thr1024Ile
NM_006772.3:c.3113C>T (SYNGAP1) MANE Select	NP_006763.2:p.Thr1038Ile
NR_174954.1:n.329+2941G>A (SYNGAP1-AS1)