Canonical Allele Identifier: CA2691774255
Gene: STXBP1 HGNC NCBI

Linked Data

Genomic Alleles

HGVS Genome Assembly
NC_000009.12:g.127675697_127675698insAAAGACCTTCCCCAA , CM000671.2:g.127675697_127675698insAAAGACCTTCCCCAA GRCh38
NC_000009.11:g.130437976_130437977insAAAGACCTTCCCCAA , CM000671.1:g.130437976_130437977insAAAGACCTTCCCCAA GRCh37
NC_000009.10:g.129477797_129477798insAAAGACCTTCCCCAA NCBI36
NG_016623.1:g.68491_68492insAAAGACCTTCCCCAA

Transcript Alleles

HGVS Amino-acid Change
ENST00000704680.1:c.1069-107_1069-106insAAAGACCTTCCCCAA ENSP00000515991.1:n.1069-107_1069-106insAAAGACCTTCCCCAA
ENST00000704681.1:c.1111-107_1111-106insAAAGACCTTCCCCAA ENSP00000515992.1:n.1111-107_1111-106insAAAGACCTTCCCCAA
ENST00000373299.5:c.1111-107_1111-106insAAAGACCTTCCCCAA MANE Select ENSP00000362396.2:n.1111-107_1111-106insAAAGACCTTCCCCAA
ENST00000373302.8:c.1111-107_1111-106insAAAGACCTTCCCCAA MANE Plus Clinical ENSP00000362399.3:n.1111-107_1111-106insAAAGACCTTCCCCAA
ENST00000626539.3:c.1069-107_1069-106insAAAGACCTTCCCCAA ENSP00000487211.2:n.1069-107_1069-106insAAAGACCTTCCCCAA
ENST00000635950.2:c.1111-107_1111-106insAAAGACCTTCCCCAA ENSP00000490903.1:n.1111-107_1111-106insAAAGACCTTCCCCAA
ENST00000636509.2:c.*66-107_*66-106insAAAGACCTTCCCCAA ENSP00000490810.1:n.*66-107_*66-106insAAAGACCTTCCCCAA
ENST00000636962.2:c.1111-107_1111-106insAAAGACCTTCCCCAA ENSP00000489762.1:n.1111-107_1111-106insAAAGACCTTCCCCAA
ENST00000637060.2:c.*753-107_*753-106insAAAGACCTTCCCCAA ENSP00000490674.2:n.*753-107_*753-106insAAAGACCTTCCCCAA
ENST00000637173.2:c.1069-107_1069-106insAAAGACCTTCCCCAA ENSP00000490519.1:n.1069-107_1069-106insAAAGACCTTCCCCAA
ENST00000637464.2:c.*1975-107_*1975-106insAAAGACCTTCCCCAA ENSP00000489655.2:n.*1975-107_*1975-106insAAAGACCTTCCCCAA
ENST00000637521.2:c.1069-107_1069-106insAAAGACCTTCCCCAA ENSP00000489791.1:n.1069-107_1069-106insAAAGACCTTCCCCAA
ENST00000637953.1:c.1111-107_1111-106insAAAGACCTTCCCCAA ENSP00000490613.1:n.1111-107_1111-106insAAAGACCTTCCCCAA
ENST00000647107.1:c.1053-107_1053-106insAAAGACCTTCCCCAA
ENST00000650920.1:c.1069-107_1069-106insAAAGACCTTCCCCAA ENSP00000498834.1:n.1069-107_1069-106insAAAGACCTTCCCCAA
ENST00000373299.4:c.1111-107_1111-106insAAAGACCTTCCCCAA ENSP00000362396.1:n.1111-107_1111-106insAAAGACCTTCCCCAA
ENST00000373302.7:c.1111-107_1111-106insAAAGACCTTCCCCAA ENSP00000362399.3:n.1111-107_1111-106insAAAGACCTTCCCCAA
ENST00000626416.2:n.947-107_947-106insAAAGACCTTCCCCAA
NM_001032221.3:c.1111-107_1111-106insAAAGACCTTCCCCAA NP_001027392.1:n.1111-107_1111-106insAAAGACCTTCCCCAA
NM_003165.3:c.1111-107_1111-106insAAAGACCTTCCCCAA NP_003156.1:n.1111-107_1111-106insAAAGACCTTCCCCAA
NM_001032221.6:c.1111-107_1111-106insAAAGACCTTCCCCAA MANE Select NP_001027392.1:n.1111-107_1111-106insAAAGACCTTCCCCAA
NM_001374306.2:c.1102-107_1102-106insAAAGACCTTCCCCAA NP_001361235.1:n.1102-107_1102-106insAAAGACCTTCCCCAA
NM_001374307.2:c.1069-107_1069-106insAAAGACCTTCCCCAA NP_001361236.1:n.1069-107_1069-106insAAAGACCTTCCCCAA
NM_001374308.2:c.1069-107_1069-106insAAAGACCTTCCCCAA NP_001361237.1:n.1069-107_1069-106insAAAGACCTTCCCCAA
NM_001374309.2:c.1069-107_1069-106insAAAGACCTTCCCCAA NP_001361238.1:n.1069-107_1069-106insAAAGACCTTCCCCAA
NM_001374310.2:c.1069-107_1069-106insAAAGACCTTCCCCAA NP_001361239.1:n.1069-107_1069-106insAAAGACCTTCCCCAA
NM_001374311.2:c.1069-107_1069-106insAAAGACCTTCCCCAA NP_001361240.1:n.1069-107_1069-106insAAAGACCTTCCCCAA
NM_001374312.2:c.1069-107_1069-106insAAAGACCTTCCCCAA NP_001361241.1:n.1069-107_1069-106insAAAGACCTTCCCCAA
NM_001374313.2:c.1111-107_1111-106insAAAGACCTTCCCCAA NP_001361242.1:n.1111-107_1111-106insAAAGACCTTCCCCAA
NM_001374314.1:c.1111-107_1111-106insAAAGACCTTCCCCAA NP_001361243.1:n.1111-107_1111-106insAAAGACCTTCCCCAA
NM_001374315.2:c.1003-107_1003-106insAAAGACCTTCCCCAA NP_001361244.1:n.1003-107_1003-106insAAAGACCTTCCCCAA
NM_003165.6:c.1111-107_1111-106insAAAGACCTTCCCCAA MANE Plus Clinical NP_003156.1:n.1111-107_1111-106insAAAGACCTTCCCCAA