Canonical Allele Identifier: CA2349707706
Gene: SNAP25 HGNC NCBI

Genomic Alleles

HGVS Genome Assembly
NC_000020.11:g.10245478T= , CM000682.2:g.10245478T= GRCh38
NC_000020.10:g.10226126T= , CM000682.1:g.10226126T= GRCh37
NC_000020.9:g.10174126T= NCBI36
NG_029626.1:g.31650T=

Transcript Alleles

HGVS Amino-acid change
ENST00000706269.1:c.-64+26265T= ENSP00000516314.1:n.-64+26265T=
ENST00000685131.1:c.-64+7452T= ENSP00000508837.1:n.-64+7452T=
ENST00000687785.1:c.-64+585T= ENSP00000510219.1:n.-64+585T=
ENST00000689077.1:n.393-29951T=
ENST00000689248.1:n.238+585T=
ENST00000689757.1:c.-108-13879T= ENSP00000509312.1:n.-108-13879T=
ENST00000689858.1:c.-64+1444T= ENSP00000510663.1:n.-64+1444T=
ENST00000690099.1:n.393-29951T=
ENST00000690766.1:n.393-29951T=
ENST00000690812.1:c.-109+1444T= ENSP00000509287.1:n.-109+1444T=
ENST00000691161.1:c.-64+18040T= ENSP00000510109.1:n.-64+18040T=
ENST00000691353.1:c.-262-20001T= ENSP00000509759.1:n.-262-20001T=
ENST00000691665.1:c.-64+11141T= ENSP00000508541.1:n.-64+11141T=
ENST00000692411.1:c.-148-15753T= ENSP00000508939.1:n.-148-15753T=
ENST00000693325.1:c.-64+18040T= ENSP00000510558.1:n.-64+18040T=
ENST00000693732.1:n.393-29951T=
ENST00000254976.7:c.-64+26501T= MANE Select ENSP00000254976.3:n.-64+26501T=
ENST00000254976.6:c.-64+26501T= ENSP00000254976.2:n.-64+26501T=
ENST00000304886.6:c.-64+26501T= ENSP00000307341.2:n.-64+26501T=
ENST00000430336.1:c.-64+26265T= ENSP00000400720.1:n.-64+26265T=
NM_003081.3:c.-64+26501T= NP_003072.2:n.-64+26501T=
NM_130811.2:c.-64+26501T= NP_570824.1:n.-64+26501T=
XM_005260808.3:c.-64+26265T= XP_005260865.1:n.-64+26265T=
XM_005260810.3:c.-64+26265T= XP_005260867.1:n.-64+26265T=
NM_001322902.1:c.-64+26265T= NP_001309831.1:n.-64+26265T=
NM_001322903.1:c.-64+11141T= NP_001309832.1:n.-64+11141T=
NM_001322904.1:c.-64+18040T= NP_001309833.1:n.-64+18040T=
NM_001322905.1:c.-64+1444T= NP_001309834.1:n.-64+1444T=
NM_001322906.1:c.-64+7452T= NP_001309835.1:n.-64+7452T=
NM_001322907.1:c.-64+18040T= NP_001309836.1:n.-64+18040T=
NM_001322908.1:c.-64+585T= NP_001309837.1:n.-64+585T=
NM_001322909.1:c.-108-13879T= NP_001309838.1:n.-108-13879T=
NM_001322910.1:c.-64+18040T= NP_001309839.1:n.-64+18040T=
NM_003081.4:c.-64+26501T= NP_003072.2:n.-64+26501T=
NM_130811.3:c.-64+26501T= NP_570824.1:n.-64+26501T=
XM_005260808.5:c.-64+26265T= XP_005260865.1:n.-64+26265T=
XM_017028021.2:c.-64+1444T= XP_016883510.1:n.-64+1444T=
XM_017028022.1:c.-64+7452T= XP_016883511.1:n.-64+7452T=
NM_001322902.2:c.-64+26265T= NP_001309831.1:n.-64+26265T=
NM_001322903.2:c.-64+11141T= NP_001309832.1:n.-64+11141T=
NM_001322904.2:c.-64+18040T= NP_001309833.1:n.-64+18040T=
NM_001322905.2:c.-64+1444T= NP_001309834.1:n.-64+1444T=
NM_001322906.2:c.-64+7452T= NP_001309835.1:n.-64+7452T=
NM_001322907.2:c.-64+18040T= NP_001309836.1:n.-64+18040T=
NM_001322908.2:c.-64+585T= NP_001309837.1:n.-64+585T=
NM_001322909.2:c.-108-13879T= NP_001309838.1:n.-108-13879T=
NM_001322910.2:c.-64+18040T= NP_001309839.1:n.-64+18040T=
NM_003081.5:c.-64+26501T= NP_003072.2:n.-64+26501T=
NM_130811.4:c.-64+26501T= MANE Select NP_570824.1:n.-64+26501T=