Canonical Allele Identifier: CA2678270777
Gene: SYNGAP1 HGNC NCBI

Linked Data

Genomic Alleles

HGVS Genome Assembly
NC_000006.12:g.33432667_33432668insTTCCC , CM000668.2:g.33432667_33432668insTTCCC GRCh38
NC_000006.11:g.33400444_33400445insTTCCC , CM000668.1:g.33400444_33400445insTTCCC GRCh37
NC_000006.10:g.33508422_33508423insTTCCC NCBI36
NG_016137.1:g.17598_17599insTTCCC
NG_016137.2:g.17598_17599insTTCCC

Transcript Alleles

HGVS Amino-acid Change
ENST00000682587.1:c.130-18_130-17insTTCCC ENSP00000507403.1:n.130-18_130-17insTTCCC
ENST00000418600.7:c.388-18_388-17insTTCCC ENSP00000403636.3:n.388-18_388-17insTTCCC
ENST00000449372.7:c.388-18_388-17insTTCCC ENSP00000416519.4:n.388-18_388-17insTTCCC
ENST00000629380.3:c.388-18_388-17insTTCCC ENSP00000486463.1:n.388-18_388-17insTTCCC
ENST00000638142.2:c.388-18_388-17insTTCCC ENSP00000490803.1:n.388-18_388-17insTTCCC
ENST00000644458.1:c.388-18_388-17insTTCCC ENSP00000495541.1:n.388-18_388-17insTTCCC
ENST00000645250.1:c.211-18_211-17insTTCCC ENSP00000494861.1:n.211-18_211-17insTTCCC
ENST00000646630.1:c.388-18_388-17insTTCCC MANE Select ENSP00000496007.1:n.388-18_388-17insTTCCC
ENST00000293748.9:c.343-18_343-17insTTCCC ENSP00000293748.6:n.343-18_343-17insTTCCC
ENST00000418600.6:c.388-18_388-17insTTCCC ENSP00000403636.3:n.388-18_388-17insTTCCC
ENST00000428982.4:c.211-18_211-17insTTCCC ENSP00000412475.2:n.211-18_211-17insTTCCC
ENST00000449372.6:c.388-18_388-17insTTCCC ENSP00000416519.3:n.388-18_388-17insTTCCC
ENST00000479510.2:n.583-18_583-17insTTCCC
ENST00000628646.2:c.388-18_388-17insTTCCC ENSP00000486431.1:n.388-18_388-17insTTCCC
ENST00000629380.2:c.388-18_388-17insTTCCC ENSP00000486463.1:n.388-18_388-17insTTCCC
NM_006772.2:c.388-18_388-17insTTCCC NP_006763.2:n.388-18_388-17insTTCCC
NM_001130066.1:c.388-18_388-17insTTCCC NP_001123538.1:n.388-18_388-17insTTCCC
NM_001130066.2:c.388-18_388-17insTTCCC NP_001123538.1:n.388-18_388-17insTTCCC
NM_006772.3:c.388-18_388-17insTTCCC MANE Select NP_006763.2:n.388-18_388-17insTTCCC