Canonical Allele Identifier: CA2770572000

Gene: SYNGAP1

Genomic Alleles

HGVS	Genome Assembly
NC_000006.12:g.33432886T>C , CM000668.2:g.33432886T>C	GRCh38
NC_000006.11:g.33400663T>C , CM000668.1:g.33400663T>C	GRCh37
NC_000006.10:g.33508641T>C	NCBI36
NG_016137.1:g.17817T>C
NG_016137.2:g.17817T>C

Transcript Alleles

HGVS	Amino-acid Change
ENST00000682587.1:c.251+80T>C	ENSP00000507403.1:n.251+80T>C
ENST00000418600.7:c.509+80T>C	ENSP00000403636.3:n.509+80T>C
ENST00000449372.7:c.509+80T>C	ENSP00000416519.4:n.509+80T>C
ENST00000629380.3:c.509+80T>C	ENSP00000486463.1:n.509+80T>C
ENST00000638142.2:c.509+80T>C	ENSP00000490803.1:n.509+80T>C
ENST00000644458.1:c.509+80T>C	ENSP00000495541.1:n.509+80T>C
ENST00000645250.1:c.332+80T>C	ENSP00000494861.1:n.332+80T>C
ENST00000646630.1:c.509+80T>C MANE Select	ENSP00000496007.1:n.509+80T>C
ENST00000293748.9:c.464+80T>C	ENSP00000293748.6:n.464+80T>C
ENST00000418600.6:c.509+80T>C	ENSP00000403636.3:n.509+80T>C
ENST00000428982.4:c.332+80T>C	ENSP00000412475.2:n.332+80T>C
ENST00000449372.6:c.509+80T>C	ENSP00000416519.3:n.509+80T>C
ENST00000479510.2:n.704+80T>C
ENST00000628646.2:c.509+80T>C	ENSP00000486431.1:n.509+80T>C
ENST00000629380.2:c.509+80T>C	ENSP00000486463.1:n.509+80T>C
NM_006772.2:c.509+80T>C	NP_006763.2:n.509+80T>C
NM_001130066.1:c.509+80T>C	NP_001123538.1:n.509+80T>C
NM_001130066.2:c.509+80T>C	NP_001123538.1:n.509+80T>C
NM_006772.3:c.509+80T>C MANE Select	NP_006763.2:n.509+80T>C