Canonical Allele Identifier: CA2349707606
Gene: SNAP25 HGNC NCBI

Genomic Alleles

HGVS Genome Assembly
NC_000020.11:g.10245250T= , CM000682.2:g.10245250T= GRCh38
NC_000020.10:g.10225898T= , CM000682.1:g.10225898T= GRCh37
NC_000020.9:g.10173898T= NCBI36
NG_029626.1:g.31422T=

Transcript Alleles

HGVS Amino-acid Change
ENST00000706269.1:c.-64+26037T= ENSP00000516314.1:n.-64+26037T=
ENST00000685131.1:c.-64+7224T= ENSP00000508837.1:n.-64+7224T=
ENST00000687785.1:c.-64+357T= ENSP00000510219.1:n.-64+357T=
ENST00000689077.1:n.393-30179T=
ENST00000689248.1:n.238+357T=
ENST00000689757.1:c.-108-14107T= ENSP00000509312.1:n.-108-14107T=
ENST00000689858.1:c.-64+1216T= ENSP00000510663.1:n.-64+1216T=
ENST00000690099.1:n.393-30179T=
ENST00000690766.1:n.393-30179T=
ENST00000690812.1:c.-109+1216T= ENSP00000509287.1:n.-109+1216T=
ENST00000691161.1:c.-64+17812T= ENSP00000510109.1:n.-64+17812T=
ENST00000691353.1:c.-262-20229T= ENSP00000509759.1:n.-262-20229T=
ENST00000691665.1:c.-64+10913T= ENSP00000508541.1:n.-64+10913T=
ENST00000692411.1:c.-148-15981T= ENSP00000508939.1:n.-148-15981T=
ENST00000693325.1:c.-64+17812T= ENSP00000510558.1:n.-64+17812T=
ENST00000693732.1:n.393-30179T=
ENST00000254976.7:c.-64+26273T= MANE Select ENSP00000254976.3:n.-64+26273T=
ENST00000254976.6:c.-64+26273T= ENSP00000254976.2:n.-64+26273T=
ENST00000304886.6:c.-64+26273T= ENSP00000307341.2:n.-64+26273T=
ENST00000430336.1:c.-64+26037T= ENSP00000400720.1:n.-64+26037T=
NM_003081.3:c.-64+26273T= NP_003072.2:n.-64+26273T=
NM_130811.2:c.-64+26273T= NP_570824.1:n.-64+26273T=
XM_005260808.3:c.-64+26037T= XP_005260865.1:n.-64+26037T=
XM_005260810.3:c.-64+26037T= XP_005260867.1:n.-64+26037T=
NM_001322902.1:c.-64+26037T= NP_001309831.1:n.-64+26037T=
NM_001322903.1:c.-64+10913T= NP_001309832.1:n.-64+10913T=
NM_001322904.1:c.-64+17812T= NP_001309833.1:n.-64+17812T=
NM_001322905.1:c.-64+1216T= NP_001309834.1:n.-64+1216T=
NM_001322906.1:c.-64+7224T= NP_001309835.1:n.-64+7224T=
NM_001322907.1:c.-64+17812T= NP_001309836.1:n.-64+17812T=
NM_001322908.1:c.-64+357T= NP_001309837.1:n.-64+357T=
NM_001322909.1:c.-108-14107T= NP_001309838.1:n.-108-14107T=
NM_001322910.1:c.-64+17812T= NP_001309839.1:n.-64+17812T=
NM_003081.4:c.-64+26273T= NP_003072.2:n.-64+26273T=
NM_130811.3:c.-64+26273T= NP_570824.1:n.-64+26273T=
XM_005260808.5:c.-64+26037T= XP_005260865.1:n.-64+26037T=
XM_017028021.2:c.-64+1216T= XP_016883510.1:n.-64+1216T=
XM_017028022.1:c.-64+7224T= XP_016883511.1:n.-64+7224T=
NM_001322902.2:c.-64+26037T= NP_001309831.1:n.-64+26037T=
NM_001322903.2:c.-64+10913T= NP_001309832.1:n.-64+10913T=
NM_001322904.2:c.-64+17812T= NP_001309833.1:n.-64+17812T=
NM_001322905.2:c.-64+1216T= NP_001309834.1:n.-64+1216T=
NM_001322906.2:c.-64+7224T= NP_001309835.1:n.-64+7224T=
NM_001322907.2:c.-64+17812T= NP_001309836.1:n.-64+17812T=
NM_001322908.2:c.-64+357T= NP_001309837.1:n.-64+357T=
NM_001322909.2:c.-108-14107T= NP_001309838.1:n.-108-14107T=
NM_001322910.2:c.-64+17812T= NP_001309839.1:n.-64+17812T=
NM_003081.5:c.-64+26273T= NP_003072.2:n.-64+26273T=
NM_130811.4:c.-64+26273T= MANE Select NP_570824.1:n.-64+26273T=