Canonical Allele Identifier: CA363682401

Gene: SYNGAP1

Linked Data - Variant Effect Evidence

Linked Data - NCBI & NCI

Genomic Alleles

HGVS	Genome Assembly
NC_000006.12:g.33435306G>T , CM000668.2:g.33435306G>T	GRCh38
NC_000006.11:g.33403083G>T , CM000668.1:g.33403083G>T	GRCh37
NC_000006.10:g.33511061G>T	NCBI36
NG_016137.1:g.20237G>T
NG_016137.2:g.20237G>T

Transcript Alleles

HGVS	Amino-acid Change
ENST00000682587.1:c.405+1G>T	ENSP00000507403.1:n.405+1G>T
ENST00000418600.7:c.663+1G>T	ENSP00000403636.3:n.663+1G>T
ENST00000449372.7:c.663+1G>T	ENSP00000416519.4:n.663+1G>T
ENST00000629380.3:c.663+1G>T	ENSP00000486463.1:n.663+1G>T
ENST00000638142.2:c.663+1G>T	ENSP00000490803.1:n.663+1G>T
ENST00000644458.1:c.663+1G>T	ENSP00000495541.1:n.663+1G>T
ENST00000645250.1:c.486+1G>T	ENSP00000494861.1:n.486+1G>T
ENST00000646630.1:c.663+1G>T MANE Select	ENSP00000496007.1:n.663+1G>T
ENST00000293748.9:c.618+1G>T	ENSP00000293748.6:n.618+1G>T
ENST00000418600.6:c.663+1G>T	ENSP00000403636.3:n.663+1G>T
ENST00000428982.4:c.486+1G>T	ENSP00000412475.2:n.486+1G>T
ENST00000449372.6:c.663+1G>T	ENSP00000416519.3:n.663+1G>T
ENST00000479510.2:n.858+1G>T
ENST00000628646.2:c.663+1G>T	ENSP00000486431.1:n.663+1G>T
ENST00000629380.2:c.663+1G>T	ENSP00000486463.1:n.663+1G>T
NM_006772.2:c.663+1G>T	NP_006763.2:n.663+1G>T
NM_001130066.1:c.663+1G>T	NP_001123538.1:n.663+1G>T
NM_001130066.2:c.663+1G>T	NP_001123538.1:n.663+1G>T
NM_006772.3:c.663+1G>T MANE Select	NP_006763.2:n.663+1G>T