Canonical Allele Identifier: CA1879919844
Gene: STXBP1 HGNC NCBI

Genomic Alleles

HGVS Genome Assembly
NC_000009.12:g.127675951_127675969delinsGTGGGACCTAGAGGAAGGC , CM000671.2:g.127675951_127675969delinsGTGGGACCTAGAGGAAGGC GRCh38
NC_000009.11:g.130438230_130438248delinsGTGGGACCTAGAGGAAGGC , CM000671.1:g.130438230_130438248delinsGTGGGACCTAGAGGAAGGC GRCh37
NC_000009.10:g.129478051_129478069delinsGTGGGACCTAGAGGAAGGC NCBI36
NG_016623.1:g.68745_68763delinsGTGGGACCTAGAGGAAGGC

Transcript Alleles

HGVS Amino-acid Change
ENST00000704680.1:c.1207+9_1207+27delinsGTGGGACCTAGAGGAAGGC ENSP00000515991.1:n.1207+9_1207+27delinsGTGGGACCTAGAGGAAGGC
ENST00000704681.1:c.1194+64_1194+82delinsGTGGGACCTAGAGGAAGGC ENSP00000515992.1:n.1194+64_1194+82delinsGTGGGACCTAGAGGAAGGC
ENST00000373299.5:c.1249+9_1249+27delinsGTGGGACCTAGAGGAAGGC MANE Select ENSP00000362396.2:n.1249+9_1249+27delinsGTGGGACCTAGAGGAAGGC
ENST00000373302.8:c.1249+9_1249+27delinsGTGGGACCTAGAGGAAGGC MANE Plus Clinical ENSP00000362399.3:n.1249+9_1249+27delinsGTGGGACCTAGAGGAAGGC
ENST00000626539.3:c.1207+9_1207+27delinsGTGGGACCTAGAGGAAGGC ENSP00000487211.2:n.1207+9_1207+27delinsGTGGGACCTAGAGGAAGGC
ENST00000635950.2:c.1249+9_1249+27delinsGTGGGACCTAGAGGAAGGC ENSP00000490903.1:n.1249+9_1249+27delinsGTGGGACCTAGAGGAAGGC
ENST00000636509.2:c.*204+9_*204+27delinsGTGGGACCTAGAGGAAGGC ENSP00000490810.1:n.*204+9_*204+27delinsGTGGGACCTAGAGGAAGGC
ENST00000636962.2:c.1249+9_1249+27delinsGTGGGACCTAGAGGAAGGC ENSP00000489762.1:n.1249+9_1249+27delinsGTGGGACCTAGAGGAAGGC
ENST00000637060.2:c.*891+9_*891+27delinsGTGGGACCTAGAGGAAGGC ENSP00000490674.2:n.*891+9_*891+27delinsGTGGGACCTAGAGGAAGGC
ENST00000637173.2:c.1207+9_1207+27delinsGTGGGACCTAGAGGAAGGC ENSP00000490519.1:n.1207+9_1207+27delinsGTGGGACCTAGAGGAAGGC
ENST00000637464.2:c.*2113+9_*2113+27delinsGTGGGACCTAGAGGAAGGC ENSP00000489655.2:n.*2113+9_*2113+27delinsGTGGGACCTAGAGGAAGGC...
ENST00000637521.2:c.1207+9_1207+27delinsGTGGGACCTAGAGGAAGGC ENSP00000489791.1:n.1207+9_1207+27delinsGTGGGACCTAGAGGAAGGC
ENST00000637953.1:c.1249+9_1249+27delinsGTGGGACCTAGAGGAAGGC ENSP00000490613.1:n.1249+9_1249+27delinsGTGGGACCTAGAGGAAGGC
ENST00000647107.1:c.1191+9_1191+27delinsGTGGGACCTAGAGGAAGGC
ENST00000650920.1:c.1207+9_1207+27delinsGTGGGACCTAGAGGAAGGC ENSP00000498834.1:n.1207+9_1207+27delinsGTGGGACCTAGAGGAAGGC
ENST00000373299.4:c.1249+9_1249+27delinsGTGGGACCTAGAGGAAGGC ENSP00000362396.1:n.1249+9_1249+27delinsGTGGGACCTAGAGGAAGGC
ENST00000373302.7:c.1249+9_1249+27delinsGTGGGACCTAGAGGAAGGC ENSP00000362399.3:n.1249+9_1249+27delinsGTGGGACCTAGAGGAAGGC
ENST00000626416.2:n.1085+9_1085+27delinsGTGGGACCTAGAGGAAGGC
NM_001032221.3:c.1249+9_1249+27delinsGTGGGACCTAGAGGAAGGC NP_001027392.1:n.1249+9_1249+27delinsGTGGGACCTAGAGGAAGGC
NM_003165.3:c.1249+9_1249+27delinsGTGGGACCTAGAGGAAGGC NP_003156.1:n.1249+9_1249+27delinsGTGGGACCTAGAGGAAGGC
NM_001032221.6:c.1249+9_1249+27delinsGTGGGACCTAGAGGAAGGC MANE Select NP_001027392.1:n.1249+9_1249+27delinsGTGGGACCTAGAGGAAGGC
NM_001374306.2:c.1240+9_1240+27delinsGTGGGACCTAGAGGAAGGC NP_001361235.1:n.1240+9_1240+27delinsGTGGGACCTAGAGGAAGGC
NM_001374307.2:c.1207+9_1207+27delinsGTGGGACCTAGAGGAAGGC NP_001361236.1:n.1207+9_1207+27delinsGTGGGACCTAGAGGAAGGC
NM_001374308.2:c.1207+9_1207+27delinsGTGGGACCTAGAGGAAGGC NP_001361237.1:n.1207+9_1207+27delinsGTGGGACCTAGAGGAAGGC
NM_001374309.2:c.1207+9_1207+27delinsGTGGGACCTAGAGGAAGGC NP_001361238.1:n.1207+9_1207+27delinsGTGGGACCTAGAGGAAGGC
NM_001374310.2:c.1207+9_1207+27delinsGTGGGACCTAGAGGAAGGC NP_001361239.1:n.1207+9_1207+27delinsGTGGGACCTAGAGGAAGGC
NM_001374311.2:c.1207+9_1207+27delinsGTGGGACCTAGAGGAAGGC NP_001361240.1:n.1207+9_1207+27delinsGTGGGACCTAGAGGAAGGC
NM_001374312.2:c.1207+9_1207+27delinsGTGGGACCTAGAGGAAGGC NP_001361241.1:n.1207+9_1207+27delinsGTGGGACCTAGAGGAAGGC
NM_001374313.2:c.1249+9_1249+27delinsGTGGGACCTAGAGGAAGGC NP_001361242.1:n.1249+9_1249+27delinsGTGGGACCTAGAGGAAGGC
NM_001374314.1:c.1249+9_1249+27delinsGTGGGACCTAGAGGAAGGC NP_001361243.1:n.1249+9_1249+27delinsGTGGGACCTAGAGGAAGGC
NM_001374315.2:c.1141+9_1141+27delinsGTGGGACCTAGAGGAAGGC NP_001361244.1:n.1141+9_1141+27delinsGTGGGACCTAGAGGAAGGC
NM_003165.6:c.1249+9_1249+27delinsGTGGGACCTAGAGGAAGGC MANE Plus Clinical NP_003156.1:n.1249+9_1249+27delinsGTGGGACCTAGAGGAAGGC