Canonical Allele Identifier: CA1879887495
Gene: STXBP1 HGNC NCBI

Genomic Alleles

HGVS Genome Assembly
NC_000009.12:g.127682410C= , CM000671.2:g.127682410C= GRCh38
NC_000009.11:g.130444689C= , CM000671.1:g.130444689C= GRCh37
NC_000009.10:g.129484510C= NCBI36
NG_016623.1:g.75204C=

Transcript Alleles

HGVS Amino-acid change
ENST00000704680.1:c.1510C= ENSP00000515991.1:p.Arg504=
ENST00000704681.1:c.1497C= ENSP00000515992.1:n.1497C=
ENST00000373299.5:c.1552C= MANE Select ENSP00000362396.2:p.Arg518=
ENST00000373302.8:c.1552C= MANE Plus Clinical ENSP00000362399.3:p.Arg518=
ENST00000626539.3:c.1510C= ENSP00000487211.2:p.Arg504=
ENST00000635950.2:c.1552C= ENSP00000490903.1:p.Arg518=
ENST00000636509.2:c.*507C= ENSP00000490810.1:n.*507C=
ENST00000636962.2:c.1552C= ENSP00000489762.1:p.Arg518=
ENST00000637060.2:c.*1194C= ENSP00000490674.2:n.*1194C=
ENST00000637173.2:c.1510C= ENSP00000490519.1:p.Arg504=
ENST00000637464.2:c.*2416C= ENSP00000489655.2:n.*2416C=
ENST00000637521.2:c.1510C= ENSP00000489791.1:p.Arg504=
ENST00000637953.1:c.1552C= ENSP00000490613.1:p.Arg518=
ENST00000647107.1:c.1494C=
ENST00000650920.1:c.1510C= ENSP00000498834.1:p.Arg504=
ENST00000373299.4:c.1552C= ENSP00000362396.1:p.Arg518=
ENST00000373302.7:c.1552C= ENSP00000362399.3:p.Arg518=
ENST00000494254.3:c.100C= ENSP00000485397.1:p.Arg34=
ENST00000626416.2:n.1388C=
ENST00000628638.1:n.144C=
NM_001032221.3:c.1552C= NP_001027392.1:p.Arg518=
NM_003165.3:c.1552C= NP_003156.1:p.Arg518=
NM_001032221.6:c.1552C= MANE Select NP_001027392.1:p.Arg518=
NM_001374306.2:c.1543C= NP_001361235.1:p.Arg515=
NM_001374307.2:c.1510C= NP_001361236.1:p.Arg504=
NM_001374308.2:c.1510C= NP_001361237.1:p.Arg504=
NM_001374309.2:c.1510C= NP_001361238.1:p.Arg504=
NM_001374310.2:c.1510C= NP_001361239.1:p.Arg504=
NM_001374311.2:c.1510C= NP_001361240.1:p.Arg504=
NM_001374312.2:c.1510C= NP_001361241.1:p.Arg504=
NM_001374313.2:c.1552C= NP_001361242.1:p.Arg518=
NM_001374314.1:c.1552C= NP_001361243.1:p.Arg518=
NM_001374315.2:c.1444C= NP_001361244.1:p.Arg482=
NM_003165.6:c.1552C= MANE Plus Clinical NP_003156.1:p.Arg518=