Canonical Allele Identifier: CA2349705211

Gene: SNAP25

Genomic Alleles

HGVS	Genome Assembly
NC_000020.11:g.10239788G= , CM000682.2:g.10239788G=	GRCh38
NC_000020.10:g.10220436G= , CM000682.1:g.10220436G=	GRCh37
NC_000020.9:g.10168436G=	NCBI36
NG_029626.1:g.25960G=

Transcript Alleles

HGVS	Amino-acid change
ENST00000706269.1:c.-64+20575G=	ENSP00000516314.1:n.-64+20575G=
ENST00000685131.1:c.-64+1762G=	ENSP00000508837.1:n.-64+1762G=
ENST00000687785.1:c.-241-4187G=	ENSP00000510219.1:n.-241-4187G=
ENST00000689077.1:n.393-35641G=
ENST00000689248.1:n.97-4964G=
ENST00000689757.1:c.-109+12350G=	ENSP00000509312.1:n.-109+12350G=
ENST00000689858.1:c.-123-4187G=	ENSP00000510663.1:n.-123-4187G=
ENST00000690099.1:n.393-35641G=
ENST00000690766.1:n.393-35641G=
ENST00000690812.1:c.-168-4187G=	ENSP00000509287.1:n.-168-4187G=
ENST00000691161.1:c.-64+12350G=	ENSP00000510109.1:n.-64+12350G=
ENST00000691353.1:c.-263+20575G=	ENSP00000509759.1:n.-263+20575G=
ENST00000691665.1:c.-64+5451G=	ENSP00000508541.1:n.-64+5451G=
ENST00000692411.1:c.-149+20811G=	ENSP00000508939.1:n.-149+20811G=
ENST00000693325.1:c.-64+12350G=	ENSP00000510558.1:n.-64+12350G=
ENST00000693732.1:n.393-35641G=
ENST00000254976.7:c.-64+20811G= MANE Select	ENSP00000254976.3:n.-64+20811G=
ENST00000254976.6:c.-64+20811G=	ENSP00000254976.2:n.-64+20811G=
ENST00000304886.6:c.-64+20811G=	ENSP00000307341.2:n.-64+20811G=
ENST00000430336.1:c.-64+20575G=	ENSP00000400720.1:n.-64+20575G=
NM_003081.3:c.-64+20811G=	NP_003072.2:n.-64+20811G=
NM_130811.2:c.-64+20811G=	NP_570824.1:n.-64+20811G=
XM_005260808.3:c.-64+20575G=	XP_005260865.1:n.-64+20575G=
XM_005260810.3:c.-64+20575G=	XP_005260867.1:n.-64+20575G=
NM_001322902.1:c.-64+20575G=	NP_001309831.1:n.-64+20575G=
NM_001322903.1:c.-64+5451G=	NP_001309832.1:n.-64+5451G=
NM_001322904.1:c.-64+12350G=	NP_001309833.1:n.-64+12350G=
NM_001322905.1:c.-123-4187G=	NP_001309834.1:n.-123-4187G=
NM_001322906.1:c.-64+1762G=	NP_001309835.1:n.-64+1762G=
NM_001322907.1:c.-64+12350G=	NP_001309836.1:n.-64+12350G=
NM_001322908.1:c.-241-4187G=	NP_001309837.1:n.-241-4187G=
NM_001322909.1:c.-108-19569G=	NP_001309838.1:n.-108-19569G=
NM_001322910.1:c.-64+12350G=	NP_001309839.1:n.-64+12350G=
NM_003081.4:c.-64+20811G=	NP_003072.2:n.-64+20811G=
NM_130811.3:c.-64+20811G=	NP_570824.1:n.-64+20811G=
XM_005260808.5:c.-64+20575G=	XP_005260865.1:n.-64+20575G=
XM_017028021.2:c.-123-4187G=	XP_016883510.1:n.-123-4187G=
XM_017028022.1:c.-64+1762G=	XP_016883511.1:n.-64+1762G=
NM_001322902.2:c.-64+20575G=	NP_001309831.1:n.-64+20575G=
NM_001322903.2:c.-64+5451G=	NP_001309832.1:n.-64+5451G=
NM_001322904.2:c.-64+12350G=	NP_001309833.1:n.-64+12350G=
NM_001322905.2:c.-123-4187G=	NP_001309834.1:n.-123-4187G=
NM_001322906.2:c.-64+1762G=	NP_001309835.1:n.-64+1762G=
NM_001322907.2:c.-64+12350G=	NP_001309836.1:n.-64+12350G=
NM_001322908.2:c.-241-4187G=	NP_001309837.1:n.-241-4187G=
NM_001322909.2:c.-108-19569G=	NP_001309838.1:n.-108-19569G=
NM_001322910.2:c.-64+12350G=	NP_001309839.1:n.-64+12350G=
NM_003081.5:c.-64+20811G=	NP_003072.2:n.-64+20811G=
NM_130811.4:c.-64+20811G= MANE Select	NP_570824.1:n.-64+20811G=