Canonical Allele Identifier: CA363636951

Gene: SYNGAP1 SYNGAP1-AS1

Linked Data

• dbSNP Id: rs1554122700
• MyVariant Identifiers: chr6:g.33414385A>T (hg19) ; chr6:g.33446608A>T (hg38)

Genomic Alleles

HGVS	Genome Assembly
NC_000006.12:g.33446608A>T , CM000668.2:g.33446608A>T	GRCh38
NC_000006.11:g.33414385A>T , CM000668.1:g.33414385A>T	GRCh37
NC_000006.10:g.33522363A>T	NCBI36
NG_016137.1:g.31539A>T
NG_016137.2:g.31539A>T

Transcript Alleles

HGVS	Amino-acid Change
ENST00000682587.1:c.3358A>T (SYNGAP1)	ENSP00000507403.1:p.Lys1120Ter
ENST00000418600.7:c.3616A>T (SYNGAP1)	ENSP00000403636.3:p.Lys1206Ter
ENST00000449372.7:c.3568A>T (SYNGAP1)	ENSP00000416519.4:p.Lys1190Ter
ENST00000629380.3:c.3616A>T (SYNGAP1)	ENSP00000486463.1:p.Lys1206Ter
ENST00000644458.1:c.3616A>T (SYNGAP1)	ENSP00000495541.1:p.Lys1206Ter
ENST00000645250.1:c.3439A>T (SYNGAP1)	ENSP00000494861.1:p.Lys1147Ter
ENST00000646630.1:c.3616A>T (SYNGAP1) MANE Select	ENSP00000496007.1:p.Lys1206Ter
ENST00000293748.9:c.3571A>T (SYNGAP1)	ENSP00000293748.6:p.Lys1191Ter
ENST00000418600.6:c.3616A>T (SYNGAP1)	ENSP00000403636.3:p.Lys1206Ter
ENST00000428982.4:c.3439A>T (SYNGAP1)	ENSP00000412475.2:p.Lys1147Ter
ENST00000449372.6:c.3568A>T (SYNGAP1)	ENSP00000416519.3:p.Lys1190Ter
ENST00000628646.2:c.3616A>T (SYNGAP1)	ENSP00000486431.1:p.Lys1206Ter
ENST00000629380.2:c.3616A>T (SYNGAP1)	ENSP00000486463.1:p.Lys1206Ter
NM_006772.2:c.3616A>T (SYNGAP1)	NP_006763.2:p.Lys1206Ter
NM_001130066.1:c.3568A>T (SYNGAP1)	NP_001123538.1:p.Lys1190Ter
NM_001130066.2:c.3568A>T (SYNGAP1)	NP_001123538.1:p.Lys1190Ter
NM_006772.3:c.3616A>T (SYNGAP1) MANE Select	NP_006763.2:p.Lys1206Ter
NR_174954.1:n.327T>A (SYNGAP1-AS1)