Canonical Allele Identifier: CA363623191

Gene: SYNGAP1 SYNGAP1-AS1

Linked Data

• MyVariant Identifiers: chr6:g.33409398A>C (hg19) ; chr6:g.33441621A>C (hg38)

Genomic Alleles

HGVS	Genome Assembly
NC_000006.12:g.33441621A>C , CM000668.2:g.33441621A>C	GRCh38
NC_000006.11:g.33409398A>C , CM000668.1:g.33409398A>C	GRCh37
NC_000006.10:g.33517376A>C	NCBI36
NG_016137.1:g.26552A>C
NG_016137.2:g.26552A>C

Transcript Alleles

HGVS	Amino-acid change
ENST00000682587.1:c.1898A>C (SYNGAP1)	ENSP00000507403.1:p.Asn633Thr
ENST00000418600.7:c.2156A>C (SYNGAP1)	ENSP00000403636.3:p.Asn719Thr
ENST00000449372.7:c.2156A>C (SYNGAP1)	ENSP00000416519.4:p.Asn719Thr
ENST00000629380.3:c.2156A>C (SYNGAP1)	ENSP00000486463.1:p.Asn719Thr
ENST00000638142.2:c.*553A>C (SYNGAP1)	ENSP00000490803.1:n.*553A>C
ENST00000644458.1:c.2156A>C (SYNGAP1)	ENSP00000495541.1:p.Asn719Thr
ENST00000645250.1:c.1979A>C (SYNGAP1)	ENSP00000494861.1:p.Asn660Thr
ENST00000646630.1:c.2156A>C (SYNGAP1) MANE Select	ENSP00000496007.1:p.Asn719Thr
ENST00000293748.9:c.2111A>C (SYNGAP1)	ENSP00000293748.6:p.Asn704Thr
ENST00000418600.6:c.2156A>C (SYNGAP1)	ENSP00000403636.3:p.Asn719Thr
ENST00000428982.4:c.1979A>C (SYNGAP1)	ENSP00000412475.2:p.Asn660Thr
ENST00000449372.6:c.2156A>C (SYNGAP1)	ENSP00000416519.3:p.Asn719Thr
ENST00000628646.2:c.2156A>C (SYNGAP1)	ENSP00000486431.1:p.Asn719Thr
ENST00000629380.2:c.2156A>C (SYNGAP1)	ENSP00000486463.1:p.Asn719Thr
NM_006772.2:c.2156A>C (SYNGAP1)	NP_006763.2:p.Asn719Thr
NM_001130066.1:c.2156A>C (SYNGAP1)	NP_001123538.1:p.Asn719Thr
NM_001130066.2:c.2156A>C (SYNGAP1)	NP_001123538.1:p.Asn719Thr
NM_006772.3:c.2156A>C (SYNGAP1) MANE Select	NP_006763.2:p.Asn719Thr
NR_174954.1:n.330-4140T>G (SYNGAP1-AS1)