Canonical Allele Identifier: CA2349707747

Gene: SNAP25

Genomic Alleles

HGVS	Genome Assembly
NC_000020.11:g.10245566_10245567delinsTG , CM000682.2:g.10245566_10245567delinsTG	GRCh38
NC_000020.10:g.10226214_10226215delinsTG , CM000682.1:g.10226214_10226215delinsTG	GRCh37
NC_000020.9:g.10174214_10174215delinsTG	NCBI36
NG_029626.1:g.31738_31739delinsTG

Transcript Alleles

HGVS	Amino-acid Change
ENST00000706269.1:c.-64+26353_-64+26354delinsTG	ENSP00000516314.1:n.-64+26353_-64+26354delinsTG
ENST00000685131.1:c.-64+7540_-64+7541delinsTG	ENSP00000508837.1:n.-64+7540_-64+7541delinsTG
ENST00000687785.1:c.-64+673_-64+674delinsTG	ENSP00000510219.1:n.-64+673_-64+674delinsTG
ENST00000689077.1:n.393-29863_393-29862delinsTG
ENST00000689248.1:n.238+673_238+674delinsTG
ENST00000689757.1:c.-108-13791_-108-13790delinsTG	ENSP00000509312.1:n.-108-13791_-108-13790delinsTG
ENST00000689858.1:c.-64+1532_-64+1533delinsTG	ENSP00000510663.1:n.-64+1532_-64+1533delinsTG
ENST00000690099.1:n.393-29863_393-29862delinsTG
ENST00000690766.1:n.393-29863_393-29862delinsTG
ENST00000690812.1:c.-109+1532_-109+1533delinsTG	ENSP00000509287.1:n.-109+1532_-109+1533delinsTG
ENST00000691161.1:c.-64+18128_-64+18129delinsTG	ENSP00000510109.1:n.-64+18128_-64+18129delinsTG
ENST00000691353.1:c.-262-19913_-262-19912delinsTG	ENSP00000509759.1:n.-262-19913_-262-19912delinsTG
ENST00000691665.1:c.-64+11229_-64+11230delinsTG	ENSP00000508541.1:n.-64+11229_-64+11230delinsTG
ENST00000692411.1:c.-148-15665_-148-15664delinsTG	ENSP00000508939.1:n.-148-15665_-148-15664delinsTG
ENST00000693325.1:c.-64+18128_-64+18129delinsTG	ENSP00000510558.1:n.-64+18128_-64+18129delinsTG
ENST00000693732.1:n.393-29863_393-29862delinsTG
ENST00000254976.7:c.-64+26589_-64+26590delinsTG MANE Select	ENSP00000254976.3:n.-64+26589_-64+26590delinsTG
ENST00000254976.6:c.-64+26589_-64+26590delinsTG	ENSP00000254976.2:n.-64+26589_-64+26590delinsTG
ENST00000304886.6:c.-64+26589_-64+26590delinsTG	ENSP00000307341.2:n.-64+26589_-64+26590delinsTG
ENST00000430336.1:c.-64+26353_-64+26354delinsTG	ENSP00000400720.1:n.-64+26353_-64+26354delinsTG
NM_003081.3:c.-64+26589_-64+26590delinsTG	NP_003072.2:n.-64+26589_-64+26590delinsTG
NM_130811.2:c.-64+26589_-64+26590delinsTG	NP_570824.1:n.-64+26589_-64+26590delinsTG
XM_005260808.3:c.-64+26353_-64+26354delinsTG	XP_005260865.1:n.-64+26353_-64+26354delinsTG
XM_005260810.3:c.-64+26353_-64+26354delinsTG	XP_005260867.1:n.-64+26353_-64+26354delinsTG
NM_001322902.1:c.-64+26353_-64+26354delinsTG	NP_001309831.1:n.-64+26353_-64+26354delinsTG
NM_001322903.1:c.-64+11229_-64+11230delinsTG	NP_001309832.1:n.-64+11229_-64+11230delinsTG
NM_001322904.1:c.-64+18128_-64+18129delinsTG	NP_001309833.1:n.-64+18128_-64+18129delinsTG
NM_001322905.1:c.-64+1532_-64+1533delinsTG	NP_001309834.1:n.-64+1532_-64+1533delinsTG
NM_001322906.1:c.-64+7540_-64+7541delinsTG	NP_001309835.1:n.-64+7540_-64+7541delinsTG
NM_001322907.1:c.-64+18128_-64+18129delinsTG	NP_001309836.1:n.-64+18128_-64+18129delinsTG
NM_001322908.1:c.-64+673_-64+674delinsTG	NP_001309837.1:n.-64+673_-64+674delinsTG
NM_001322909.1:c.-108-13791_-108-13790delinsTG	NP_001309838.1:n.-108-13791_-108-13790delinsTG
NM_001322910.1:c.-64+18128_-64+18129delinsTG	NP_001309839.1:n.-64+18128_-64+18129delinsTG
NM_003081.4:c.-64+26589_-64+26590delinsTG	NP_003072.2:n.-64+26589_-64+26590delinsTG
NM_130811.3:c.-64+26589_-64+26590delinsTG	NP_570824.1:n.-64+26589_-64+26590delinsTG
XM_005260808.5:c.-64+26353_-64+26354delinsTG	XP_005260865.1:n.-64+26353_-64+26354delinsTG
XM_017028021.2:c.-64+1532_-64+1533delinsTG	XP_016883510.1:n.-64+1532_-64+1533delinsTG
XM_017028022.1:c.-64+7540_-64+7541delinsTG	XP_016883511.1:n.-64+7540_-64+7541delinsTG
NM_001322902.2:c.-64+26353_-64+26354delinsTG	NP_001309831.1:n.-64+26353_-64+26354delinsTG
NM_001322903.2:c.-64+11229_-64+11230delinsTG	NP_001309832.1:n.-64+11229_-64+11230delinsTG
NM_001322904.2:c.-64+18128_-64+18129delinsTG	NP_001309833.1:n.-64+18128_-64+18129delinsTG
NM_001322905.2:c.-64+1532_-64+1533delinsTG	NP_001309834.1:n.-64+1532_-64+1533delinsTG
NM_001322906.2:c.-64+7540_-64+7541delinsTG	NP_001309835.1:n.-64+7540_-64+7541delinsTG
NM_001322907.2:c.-64+18128_-64+18129delinsTG	NP_001309836.1:n.-64+18128_-64+18129delinsTG
NM_001322908.2:c.-64+673_-64+674delinsTG	NP_001309837.1:n.-64+673_-64+674delinsTG
NM_001322909.2:c.-108-13791_-108-13790delinsTG	NP_001309838.1:n.-108-13791_-108-13790delinsTG
NM_001322910.2:c.-64+18128_-64+18129delinsTG	NP_001309839.1:n.-64+18128_-64+18129delinsTG
NM_003081.5:c.-64+26589_-64+26590delinsTG	NP_003072.2:n.-64+26589_-64+26590delinsTG
NM_130811.4:c.-64+26589_-64+26590delinsTG MANE Select	NP_570824.1:n.-64+26589_-64+26590delinsTG