Canonical Allele Identifier: CA2578585376
Gene: SYNGAP1 HGNC NCBI

Linked Data

Genomic Alleles

HGVS Genome Assembly
NC_000006.12:g.33435097_33435100del , CM000668.2:g.33435097_33435100del GRCh38
NC_000006.11:g.33402874_33402877del , CM000668.1:g.33402874_33402877del GRCh37
NC_000006.10:g.33510852_33510855del NCBI36
NG_016137.1:g.20028_20031del
NG_016137.2:g.20028_20031del

Transcript Alleles

HGVS Amino-acid Change
ENST00000682587.1:c.252-55_252-52del ENSP00000507403.1:n.252-55_252-52del
ENST00000418600.7:c.510-55_510-52del ENSP00000403636.3:n.510-55_510-52del
ENST00000449372.7:c.510-55_510-52del ENSP00000416519.4:n.510-55_510-52del
ENST00000629380.3:c.510-55_510-52del ENSP00000486463.1:n.510-55_510-52del
ENST00000638142.2:c.510-55_510-52del ENSP00000490803.1:n.510-55_510-52del
ENST00000644458.1:c.510-55_510-52del ENSP00000495541.1:n.510-55_510-52del
ENST00000645250.1:c.333-55_333-52del ENSP00000494861.1:n.333-55_333-52del
ENST00000646630.1:c.510-55_510-52del MANE Select ENSP00000496007.1:n.510-55_510-52del
ENST00000293748.9:c.465-55_465-52del ENSP00000293748.6:n.465-55_465-52del
ENST00000418600.6:c.510-55_510-52del ENSP00000403636.3:n.510-55_510-52del
ENST00000428982.4:c.333-55_333-52del ENSP00000412475.2:n.333-55_333-52del
ENST00000449372.6:c.510-55_510-52del ENSP00000416519.3:n.510-55_510-52del
ENST00000479510.2:n.705-55_705-52del
ENST00000628646.2:c.510-55_510-52del ENSP00000486431.1:n.510-55_510-52del
ENST00000629380.2:c.510-55_510-52del ENSP00000486463.1:n.510-55_510-52del
NM_006772.2:c.510-55_510-52del NP_006763.2:n.510-55_510-52del
NM_001130066.1:c.510-55_510-52del NP_001123538.1:n.510-55_510-52del
NM_001130066.2:c.510-55_510-52del NP_001123538.1:n.510-55_510-52del
NM_006772.3:c.510-55_510-52del MANE Select NP_006763.2:n.510-55_510-52del