Canonical Allele Identifier: CA1879919949

Gene: STXBP1

Genomic Alleles

HGVS	Genome Assembly
NC_000009.12:g.127676076_127676077delinsCT , CM000671.2:g.127676076_127676077delinsCT	GRCh38
NC_000009.11:g.130438355_130438356delinsCT , CM000671.1:g.130438355_130438356delinsCT	GRCh37
NC_000009.10:g.129478176_129478177delinsCT	NCBI36
NG_016623.1:g.68870_68871delinsCT

Transcript Alleles

HGVS	Amino-acid Change
ENST00000704680.1:c.1207+134_1207+135delinsCT	ENSP00000515991.1:n.1207+134_1207+135delinsCT
ENST00000704681.1:c.1194+189_1194+190delinsCT	ENSP00000515992.1:n.1194+189_1194+190delinsCT
ENST00000373299.5:c.1249+134_1249+135delinsCT MANE Select	ENSP00000362396.2:n.1249+134_1249+135delinsCT
ENST00000373302.8:c.1249+134_1249+135delinsCT MANE Plus Clinical	ENSP00000362399.3:n.1249+134_1249+135delinsCT
ENST00000626539.3:c.1207+134_1207+135delinsCT	ENSP00000487211.2:n.1207+134_1207+135delinsCT
ENST00000635950.2:c.1249+134_1249+135delinsCT	ENSP00000490903.1:n.1249+134_1249+135delinsCT
ENST00000636509.2:c.*204+134_*204+135delinsCT	ENSP00000490810.1:n.*204+134_*204+135delinsCT
ENST00000636962.2:c.1249+134_1249+135delinsCT	ENSP00000489762.1:n.1249+134_1249+135delinsCT
ENST00000637060.2:c.*891+134_*891+135delinsCT	ENSP00000490674.2:n.*891+134_*891+135delinsCT
ENST00000637173.2:c.1207+134_1207+135delinsCT	ENSP00000490519.1:n.1207+134_1207+135delinsCT
ENST00000637464.2:c.*2113+134_*2113+135delinsCT	ENSP00000489655.2:n.*2113+134_*2113+135delinsCT
ENST00000637521.2:c.1207+134_1207+135delinsCT	ENSP00000489791.1:n.1207+134_1207+135delinsCT
ENST00000637953.1:c.1249+134_1249+135delinsCT	ENSP00000490613.1:n.1249+134_1249+135delinsCT
ENST00000647107.1:c.1191+134_1191+135delinsCT
ENST00000650920.1:c.1207+134_1207+135delinsCT	ENSP00000498834.1:n.1207+134_1207+135delinsCT
ENST00000373299.4:c.1249+134_1249+135delinsCT	ENSP00000362396.1:n.1249+134_1249+135delinsCT
ENST00000373302.7:c.1249+134_1249+135delinsCT	ENSP00000362399.3:n.1249+134_1249+135delinsCT
ENST00000626416.2:n.1085+134_1085+135delinsCT
NM_001032221.3:c.1249+134_1249+135delinsCT	NP_001027392.1:n.1249+134_1249+135delinsCT
NM_003165.3:c.1249+134_1249+135delinsCT	NP_003156.1:n.1249+134_1249+135delinsCT
NM_001032221.6:c.1249+134_1249+135delinsCT MANE Select	NP_001027392.1:n.1249+134_1249+135delinsCT
NM_001374306.2:c.1240+134_1240+135delinsCT	NP_001361235.1:n.1240+134_1240+135delinsCT
NM_001374307.2:c.1207+134_1207+135delinsCT	NP_001361236.1:n.1207+134_1207+135delinsCT
NM_001374308.2:c.1207+134_1207+135delinsCT	NP_001361237.1:n.1207+134_1207+135delinsCT
NM_001374309.2:c.1207+134_1207+135delinsCT	NP_001361238.1:n.1207+134_1207+135delinsCT
NM_001374310.2:c.1207+134_1207+135delinsCT	NP_001361239.1:n.1207+134_1207+135delinsCT
NM_001374311.2:c.1207+134_1207+135delinsCT	NP_001361240.1:n.1207+134_1207+135delinsCT
NM_001374312.2:c.1207+134_1207+135delinsCT	NP_001361241.1:n.1207+134_1207+135delinsCT
NM_001374313.2:c.1249+134_1249+135delinsCT	NP_001361242.1:n.1249+134_1249+135delinsCT
NM_001374314.1:c.1249+134_1249+135delinsCT	NP_001361243.1:n.1249+134_1249+135delinsCT
NM_001374315.2:c.1141+134_1141+135delinsCT	NP_001361244.1:n.1141+134_1141+135delinsCT
NM_003165.6:c.1249+134_1249+135delinsCT MANE Plus Clinical	NP_003156.1:n.1249+134_1249+135delinsCT