Canonical Allele Identifier: CA2678270152
Gene: SYNGAP1 HGNC NCBI

Linked Data

Genomic Alleles

HGVS Genome Assembly
NC_000006.12:g.33432651_33432652insGCCCCCCCCCCCCCC , CM000668.2:g.33432651_33432652insGCCCCCCCCCCCCCC GRCh38
NC_000006.11:g.33400428_33400429insGCCCCCCCCCCCCCC , CM000668.1:g.33400428_33400429insGCCCCCCCCCCCCCC GRCh37
NC_000006.10:g.33508406_33508407insGCCCCCCCCCCCCCC NCBI36
NG_016137.1:g.17582_17583insGCCCCCCCCCCCCCC
NG_016137.2:g.17582_17583insGCCCCCCCCCCCCCC

Transcript Alleles

HGVS Amino-acid Change
ENST00000682587.1:c.130-34_130-33insGCCCCCCCCCCCCCC ENSP00000507403.1:n.130-34_130-33insGCCCCCCCCCCCCCC
ENST00000418600.7:c.388-34_388-33insGCCCCCCCCCCCCCC ENSP00000403636.3:n.388-34_388-33insGCCCCCCCCCCCCCC
ENST00000449372.7:c.388-34_388-33insGCCCCCCCCCCCCCC ENSP00000416519.4:n.388-34_388-33insGCCCCCCCCCCCCCC
ENST00000629380.3:c.388-34_388-33insGCCCCCCCCCCCCCC ENSP00000486463.1:n.388-34_388-33insGCCCCCCCCCCCCCC
ENST00000638142.2:c.388-34_388-33insGCCCCCCCCCCCCCC ENSP00000490803.1:n.388-34_388-33insGCCCCCCCCCCCCCC
ENST00000644458.1:c.388-34_388-33insGCCCCCCCCCCCCCC ENSP00000495541.1:n.388-34_388-33insGCCCCCCCCCCCCCC
ENST00000645250.1:c.211-34_211-33insGCCCCCCCCCCCCCC ENSP00000494861.1:n.211-34_211-33insGCCCCCCCCCCCCCC
ENST00000646630.1:c.388-34_388-33insGCCCCCCCCCCCCCC MANE Select ENSP00000496007.1:n.388-34_388-33insGCCCCCCCCCCCCCC
ENST00000293748.9:c.343-34_343-33insGCCCCCCCCCCCCCC ENSP00000293748.6:n.343-34_343-33insGCCCCCCCCCCCCCC
ENST00000418600.6:c.388-34_388-33insGCCCCCCCCCCCCCC ENSP00000403636.3:n.388-34_388-33insGCCCCCCCCCCCCCC
ENST00000428982.4:c.211-34_211-33insGCCCCCCCCCCCCCC ENSP00000412475.2:n.211-34_211-33insGCCCCCCCCCCCCCC
ENST00000449372.6:c.388-34_388-33insGCCCCCCCCCCCCCC ENSP00000416519.3:n.388-34_388-33insGCCCCCCCCCCCCCC
ENST00000479510.2:n.583-34_583-33insGCCCCCCCCCCCCCC
ENST00000628646.2:c.388-34_388-33insGCCCCCCCCCCCCCC ENSP00000486431.1:n.388-34_388-33insGCCCCCCCCCCCCCC
ENST00000629380.2:c.388-34_388-33insGCCCCCCCCCCCCCC ENSP00000486463.1:n.388-34_388-33insGCCCCCCCCCCCCCC
NM_006772.2:c.388-34_388-33insGCCCCCCCCCCCCCC NP_006763.2:n.388-34_388-33insGCCCCCCCCCCCCCC
NM_001130066.1:c.388-34_388-33insGCCCCCCCCCCCCCC NP_001123538.1:n.388-34_388-33insGCCCCCCCCCCCCCC
NM_001130066.2:c.388-34_388-33insGCCCCCCCCCCCCCC NP_001123538.1:n.388-34_388-33insGCCCCCCCCCCCCCC
NM_006772.3:c.388-34_388-33insGCCCCCCCCCCCCCC MANE Select NP_006763.2:n.388-34_388-33insGCCCCCCCCCCCCCC