Canonical Allele Identifier: CA566700764
Gene: SYNGAP1 HGNC NCBI
SYNGAP1-AS1 HGNC NCBI

Linked Data

dbSNP Id: rs1425256898

Genomic Alleles

HGVS Genome Assembly
NC_000006.12:g.33446546_33446547del , CM000668.2:g.33446546_33446547del GRCh38
NC_000006.11:g.33414323_33414324del , CM000668.1:g.33414323_33414324del GRCh37
NC_000006.10:g.33522301_33522302del NCBI36
NG_016137.1:g.31477_31478del
NG_016137.2:g.31477_31478del

Transcript Alleles

HGVS Amino-acid Change
ENST00000682587.1:c.3325-29_3325-28del (SYNGAP1) ENSP00000507403.1:n.3325-29_3325-28del
ENST00000418600.7:c.3583-29_3583-28del (SYNGAP1) ENSP00000403636.3:n.3583-29_3583-28del
ENST00000449372.7:c.3541-35_3541-34del (SYNGAP1) ENSP00000416519.4:n.3541-35_3541-34del
ENST00000629380.3:c.3583-29_3583-28del (SYNGAP1) ENSP00000486463.1:n.3583-29_3583-28del
ENST00000644458.1:c.3583-29_3583-28del (SYNGAP1) ENSP00000495541.1:n.3583-29_3583-28del
ENST00000645250.1:c.3406-29_3406-28del (SYNGAP1) ENSP00000494861.1:n.3406-29_3406-28del
ENST00000646630.1:c.3583-29_3583-28del (SYNGAP1) MANE Select ENSP00000496007.1:n.3583-29_3583-28del
ENST00000293748.9:c.3538-29_3538-28del (SYNGAP1) ENSP00000293748.6:n.3538-29_3538-28del
ENST00000418600.6:c.3583-29_3583-28del (SYNGAP1) ENSP00000403636.3:n.3583-29_3583-28del
ENST00000428982.4:c.3406-29_3406-28del (SYNGAP1) ENSP00000412475.2:n.3406-29_3406-28del
ENST00000449372.6:c.3541-35_3541-34del (SYNGAP1) ENSP00000416519.3:n.3541-35_3541-34del
ENST00000628646.2:c.3583-29_3583-28del (SYNGAP1) ENSP00000486431.1:n.3583-29_3583-28del
ENST00000629380.2:c.3583-29_3583-28del (SYNGAP1) ENSP00000486463.1:n.3583-29_3583-28del
NM_006772.2:c.3583-29_3583-28del (SYNGAP1) NP_006763.2:n.3583-29_3583-28del
NM_001130066.1:c.3541-35_3541-34del (SYNGAP1) NP_001123538.1:n.3541-35_3541-34del
NM_001130066.2:c.3541-35_3541-34del (SYNGAP1) NP_001123538.1:n.3541-35_3541-34del
NM_006772.3:c.3583-29_3583-28del (SYNGAP1) MANE Select NP_006763.2:n.3583-29_3583-28del
NR_174954.1:n.329+60_329+61del (SYNGAP1-AS1)