Canonical Allele Identifier: CA2736283212

Gene: SNAP25

Linked Data

• dbSNP Id: rs2122726952

Genomic Alleles

HGVS	Genome Assembly
NC_000020.11:g.10239872del , CM000682.2:g.10239872del	GRCh38
NC_000020.10:g.10220520del , CM000682.1:g.10220520del	GRCh37
NC_000020.9:g.10168520del	NCBI36
NG_029626.1:g.26044del

Transcript Alleles

HGVS	Amino-acid change
ENST00000706269.1:c.-64+20659del	ENSP00000516314.1:n.-64+20659del
ENST00000685131.1:c.-64+1846del	ENSP00000508837.1:n.-64+1846del
ENST00000687785.1:c.-241-4103del	ENSP00000510219.1:n.-241-4103del
ENST00000689077.1:n.393-35557del
ENST00000689248.1:n.97-4880del
ENST00000689757.1:c.-109+12434del	ENSP00000509312.1:n.-109+12434del
ENST00000689858.1:c.-123-4103del	ENSP00000510663.1:n.-123-4103del
ENST00000690099.1:n.393-35557del
ENST00000690766.1:n.393-35557del
ENST00000690812.1:c.-168-4103del	ENSP00000509287.1:n.-168-4103del
ENST00000691161.1:c.-64+12434del	ENSP00000510109.1:n.-64+12434del
ENST00000691353.1:c.-263+20659del	ENSP00000509759.1:n.-263+20659del
ENST00000691665.1:c.-64+5535del	ENSP00000508541.1:n.-64+5535del
ENST00000692411.1:c.-149+20895del	ENSP00000508939.1:n.-149+20895del
ENST00000693325.1:c.-64+12434del	ENSP00000510558.1:n.-64+12434del
ENST00000693732.1:n.393-35557del
ENST00000254976.7:c.-64+20895del MANE Select	ENSP00000254976.3:n.-64+20895del
ENST00000254976.6:c.-64+20895del	ENSP00000254976.2:n.-64+20895del
ENST00000304886.6:c.-64+20895del	ENSP00000307341.2:n.-64+20895del
ENST00000430336.1:c.-64+20659del	ENSP00000400720.1:n.-64+20659del
NM_003081.3:c.-64+20895del	NP_003072.2:n.-64+20895del
NM_130811.2:c.-64+20895del	NP_570824.1:n.-64+20895del
XM_005260808.3:c.-64+20659del	XP_005260865.1:n.-64+20659del
XM_005260810.3:c.-64+20659del	XP_005260867.1:n.-64+20659del
NM_001322902.1:c.-64+20659del	NP_001309831.1:n.-64+20659del
NM_001322903.1:c.-64+5535del	NP_001309832.1:n.-64+5535del
NM_001322904.1:c.-64+12434del	NP_001309833.1:n.-64+12434del
NM_001322905.1:c.-123-4103del	NP_001309834.1:n.-123-4103del
NM_001322906.1:c.-64+1846del	NP_001309835.1:n.-64+1846del
NM_001322907.1:c.-64+12434del	NP_001309836.1:n.-64+12434del
NM_001322908.1:c.-241-4103del	NP_001309837.1:n.-241-4103del
NM_001322909.1:c.-108-19485del	NP_001309838.1:n.-108-19485del
NM_001322910.1:c.-64+12434del	NP_001309839.1:n.-64+12434del
NM_003081.4:c.-64+20895del	NP_003072.2:n.-64+20895del
NM_130811.3:c.-64+20895del	NP_570824.1:n.-64+20895del
XM_005260808.5:c.-64+20659del	XP_005260865.1:n.-64+20659del
XM_017028021.2:c.-123-4103del	XP_016883510.1:n.-123-4103del
XM_017028022.1:c.-64+1846del	XP_016883511.1:n.-64+1846del
NM_001322902.2:c.-64+20659del	NP_001309831.1:n.-64+20659del
NM_001322903.2:c.-64+5535del	NP_001309832.1:n.-64+5535del
NM_001322904.2:c.-64+12434del	NP_001309833.1:n.-64+12434del
NM_001322905.2:c.-123-4103del	NP_001309834.1:n.-123-4103del
NM_001322906.2:c.-64+1846del	NP_001309835.1:n.-64+1846del
NM_001322907.2:c.-64+12434del	NP_001309836.1:n.-64+12434del
NM_001322908.2:c.-241-4103del	NP_001309837.1:n.-241-4103del
NM_001322909.2:c.-108-19485del	NP_001309838.1:n.-108-19485del
NM_001322910.2:c.-64+12434del	NP_001309839.1:n.-64+12434del
NM_003081.5:c.-64+20895del	NP_003072.2:n.-64+20895del
NM_130811.4:c.-64+20895del MANE Select	NP_570824.1:n.-64+20895del